Covonia Chesty Cough Mixture Mentholated
 

Pills
 

ED Pills

ED Drugs
 

Covonia Chesty Cough Mixture Mentholated


1. Name Of The Medicinal Product

Covonia Chesty Cough Mixture Mentholated

2. Qualitative And Quantitative Composition

Levomenthol

4.0mg/5ml

Squill Tincture

0.6ml/5ml

Liquorice Liquid Extract

0.125ml/5ml

For excipients, see 6.1

3. Pharmaceutical Form

Oral solution.

A brown, viscous, opaque liquid

4. Clinical Particulars 4.1 Therapeutic Indications

For the symptomatic relief of productive (chesty) coughs and sore throats.

4.2 Posology And Method Of Administration

Oral.

Recommended Doses

Adults, the elderly and children over 12 years: One or two 5ml spoonfuls.

Children 5-12 years: One 5ml spoonful.

Dosage Schedule

The dose to be taken every four hours if required.

4.3 Contraindications

Contraindicated in patients with known hypersensitivity to any of the ingredients. Also Contraindicated in patients with cardiac disorders.

4.4 Special Warnings And Precautions For Use

If symptoms persist or worsen consult your doctor.

Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine as it contains sucrose and glucose.

This medicine contains up to 600mg ethanol per 10ml dose. Harmful for those suffering from alcoholism. To be taken into account in pregnant or breastfeeding women, children and high-risk groups such as people with liver disease or epilepsy.

May cause allergic reactions, possibly delayed as this medicine contains sodium methyl, ethyl and propyl hydroxybenzoates (E219, E215 and E217)

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

Toxicity of squill glycosides may be increased when given in combination with thiazides or loop diuretics, as these may cause hypokalaemia and hypomagnesaemia, which may lead to cardiac arrhythmias.

When used with carbenoxolone it may produce sodium and water retention and hypokalaemia. and may give rise to greater toxicity of squill.

4.6 Pregnancy And Lactation

There are no adverse reports when used in recommended doses.

However, as with all medicines care should be taken when using this product in pregnancy and medical advice sought if necessary.

4.7 Effects On Ability To Drive And Use Machines

None.

4.8 Undesirable Effects

No adverse effects have been reported with this product, however, a few cases of hypersensitivity reactions to menthol have been reported. These include generalised urticaria and flushing, menthol may give rise to contact dermatitis.

Liquorice may cause sodium and water retention, and hypokalaemia.

4.9 Overdose

Ingestion of large doses of the active ingredients has been reported to cause the following effects: Gastrointestinal disturbances such as abdominal pain, nausea, vomiting and diarrhoea would be expected to occur with the menthol and squill.

Common symptoms of digoxin overdosage include headache, facial pain, fatigue, weakness, dizziness, drowsiness, disorientation, mental confusion, bad dreams and more rarely delirium, acute psychoses, and hallucinations. Convulsions have been reported. Visual disturbances including blurred vision may occur. Colour vision may be affected with objects appearing yellow or less frequently green, red, brown, blue or white.

Adverse effects on the heart may result from the cardiac glycosides in squill. Toxic doses may cause or aggravate heart failure. Supraventricular or ventricular arrhythmias and defects of conduction are common and may be an early indication of excessive dosage.

In addition CNS effects such as vertigo, ataxia and drowsiness have been reported after ingestion of large quantities of menthol; reported adverse effects following excessive ingestion of liquorice include hypertension, congestive heart failure, cardiac arrest, headache, muscle weakness, myopathy, myoglobinuria, paralysis, hyperprolactinaemia and amenorrhoea.

In the unlikely event of overdosage with this preparation, gastric lavage and / or symptomatic treatment together with supportive measures should be employed. Treatment of acute digoxin poisoning consists of emptying the stomach by emesis or lavage. Activated charcoal may be given. Cardiac toxicity should be treated under ECG control and serum electrolytes should be monitored. Anti-arrhythmic treatment may be necessary and should be determined by the specific arrhythmia present. Atropine may be given intravenously to control bradycardia and in patients with heart block; cardiac pacing may be necessary if atropine is not effective. Colestyramine or colestipol may be of use in increasing the elimination of cardiac glycosides.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

R05C – Cough and cold preparations, expectorants, excl. combinations with cough suppressants

Menthol dilates the blood vessels causing a sensation of coldness followed by analgesic effect. It is used to relieve the symptoms of bronchitis, sinusitis and similar conditions.

Squill has an irritant effect on the gastric mucosa, it has a reflex expectorant action.

Liquorice is a demulcent and mild expectorant.

5.2 Pharmacokinetic Properties

After absorption menthol is excreted in the bile and urine as a glucuronide.

Squill glycosides are poorly absorbed from the gastro-intestinal tract, they are of short acting duration and are not cumulative, they are excreted in the urine and faeces.

No information is available on the pharmacokinetics of liquorice.

5.3 Preclinical Safety Data

None.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Peppermint oil, anise oil, capsicum tincture capsicum oleoresin, ethanol), sucrose, liquid glucose, magnesium aluminium silicate, sodium nipasept (E215, E217, E219), glycerol (E422), caramel (E150) and purified water.

6.2 Incompatibilities

None known.

6.3 Shelf Life

50ml : 36 months unopened.

150ml: 36 months unopened.

180ml: 36 months unopened.

200ml: 36 months unopened.

300ml: 36 months unopened.

6.4 Special Precautions For Storage

Do not store above 25°C.

6.5 Nature And Contents Of Container

50ml: Amber glass bottle with white 28mm cap with tamper evident band and EPE/ Saranex liner.

150ml: Amber glass bottle with white 28mm cap with tamper evident band and EPE/ Saranex liner.

180ml: Amber glass bottle with white 28mm cap with tamper evident band and EPE/ Saranex liner.

200ml: Amber glass bottle with white 28mm cap with tamper evident band and EPE/ Saranex liner.

300ml: Amber glass bottle with white 28mm cap with tamper evident band and EPE/ Saranex liner.

6.6 Special Precautions For Disposal And Other Handling

None

7. Marketing Authorisation Holder

Thornton & Ross Ltd

Linthwaite Laboratories

Huddersfield

HD7 5QH

United Kingdom

8. Marketing Authorisation Number(S)

PL 00240/0047

9. Date Of First Authorisation/Renewal Of The Authorisation

12/09/2007

10. Date Of Revision Of The Text

15/02/2011


Download




Covonia Catarrh Relief Formula


1. Name Of The Medicinal Product

Covonia Catarrh Relief Formula

2. Qualitative And Quantitative Composition

Each 5ml contains:-

Liquid Extract Boneset (1:1 21% alcohol) 0.6ml

Liquid Extract Blue Flag (1:1 37% alcohol) 0.05ml

Liquid Extract Burdock Root (1:1 21% alcohol) 0.25ml

Liquid Extract Hyssop (1:1 21% alcohol) 0.35ml

3. Pharmaceutical Form

Oral Liquid

4. Clinical Particulars 4.1 Therapeutic Indications

A herbal remedy traditionally used for the symptomatic relief of nasal catarrh and catarrh of the throat.

4.2 Posology And Method Of Administration

Adults and the Elderly (only): One 5ml spoonful three times a day.

Children over 12: One 5ml spoonful morning and evening

Children under 12: Not recommended

4.3 Contraindications

Hypersensitivity to any of the ingredients.

4.4 Special Warnings And Precautions For Use

This medicinal product contains 11.5 vol% ethanol (alcohol), i.e. up to 453 mg per dose, equivalent to 12 ml beer, 5 ml wine per dose.

Harmful for those suffering from alcoholism.

To be taken into account in pregnant or breast-feeding women, children and high-risk groups such as patients with liver disease, or epilepsy.

Patients with rare glucose-galactose malabsorption should not take this medicine.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

Refer to 4.4

4.6 Pregnancy And Lactation

There are no adequate data from the use of Covonia Catarrh Relief Formula in pregnant women. Covonia Catarrh Relief Formula should not be used in pregnancy.

4.7 Effects On Ability To Drive And Use Machines

None

4.8 Undesirable Effects

None

4.9 Overdose

No cases known.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

Boneset and Hyssop are specific herbal anticatarrhals. Boneset is also immune-stimulant.

5.2 Pharmacokinetic Properties

No information available.

5.3 Preclinical Safety Data

No information available.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Chloroform spirit (containing chloroform, ethanol and purified water), methyl parahydroxybenzoate (E218), tincture capsicum (containing capsicum oleoresin, ethanol and water), colour solution (containing nipagen m, caramel (E150), glycerol (E422), chloroform, water), viscarin SD 389 (contains dextrose/carageenan (E407)), menthol, sodium saccharin (E954), and purified water.

6.2 Incompatibilities

None.

6.3 Shelf Life

Three years unopened.

Once opened use within 28 days.

6.4 Special Precautions For Storage

Do not store above 25 degrees C.

6.5 Nature And Contents Of Container

100ml amber glass sirop bottle with 28mm polypropylene white tamper-evident cap with EPE/Aluminium/Melinex liner.

150ml amber glass bottle embossed “Covonia” with a 28mm polypropylene white tamper evident cap with EPE/Aluminium/Melinex liner.

6.6 Special Precautions For Disposal And Other Handling

Not applicable.

7. Marketing Authorisation Holder

Thornton & Ross Ltd

Linthwaite, Huddersfield

West Yorkshire HD7 5QH

United Kingdom

8. Marketing Authorisation Number(S)

PL 00240/0142

9. Date Of First Authorisation/Renewal Of The Authorisation

22/02/2006

10. Date Of Revision Of The Text

04/10/2010


Download




Boots Nirolex Chesty Cough & Congestion Relief Linctus


Boots Nirolex Chesty Cough & Congestion Relief Linctus (Guaifenesin, Pseudoephedrine Hydrochloride)

Non drowsy

Relieves chesty coughs

Clears nasal congestion

120 ml e

Read all of this carton for full instructions.

What this medicine is for

This medicine contains Guaifenesin and Pseudoephedrine Hydrochloride, which act to relieve coughs and blocked noses.

It can be used to relieve the symptoms of chesty coughs, catarrh and blocked noses, without causing drowsiness.

Before you take this medicine Do not take: If you are allergic to any of the ingredients If you have heart or blood vessel disease, high blood pressure (including that due to a tumour near your kidney), glaucoma If you have severe kidney problems, diabetes, an overactive thyroid If you are taking monoamine oxidase inhibitors (for depression) or have taken them in the last 14 days If you have an intolerance to some sugars, unless your doctor tells you to (this medicine contains sucrose) If you are a man with prostate problems If you are pregnant Talk to your pharmacist or doctor: If you have other kidney problems (see above) If you take other medicines tricyclic antidepressants digoxin (for heart problems) medicines for high blood pressure other decongestants appetite suppressants or stimulants If you are breastfeeding Information about some of the ingredients:

The colour carmoisine (E122) in this medicine may cause allergic reactions.

How to take this medicine

Check the seal is not broken before first use. If it is, do not take the medicine.

Adults and children of 12 years and over
Take two 5ml spoonfuls 4 times a day.

Children of 6 to 11 years
Take one 5ml spoonful 3 times a day.

This medicine should be swallowed.

Do not give to children under 6 years.

Warning: Do not exceed the stated dose

If symptoms do not go away talk to your doctor.

If you take too much: Talk to doctor straight away.

Possible side effects

Most people will not have problems, but some may get some of these:

Feeling sick, being sick, stomach discomfort Headache Irritability, restlessness, confusion, shaking, difficulty sleeping, dizziness Fast heart beat, heart rhythm problems, palpitations, high blood pressure Difficulty in passing urine Skin rashes

If any side effect becomes severe, or you notice any side effect not listed here, please tell your pharmacist or doctor.

How to store this medicine

Do not store above 30°C.

Keep all medicines out of the sight and reach of children.

Use by the date on the end flap of the carton.

Active ingredients

Each 5 ml of oral solution contains Guaifenesin 100 mg, Pseudoephedrine Hydrochloride 30 mg.

Also contains: purified water, liquid sugar (sucrose), glycerol (E422), citric acid, sodium citrate, hyetellose, potassium sorbate (E202), acesulfame potassium, carmoisine (E122), patent V (E131), flavours (strawberry, blackcurrant, menthol, cream).

PL 00014/0555 [P]

Text prepared 11/07

Manufactured by the Marketing Authorisation holder The Boots Company PLC Nottingham England NG2 3AA Other formats

To request a copy of this carton in Braille, large print or audio please call, free of charge:

0800 198 5000 (UK only)

Please be ready to give the following information:

Product name: Boots Nirolex Chesty Cough & Congestion Relief Linctus

Reference number: 00014/0555

This is a service provided by the Royal National Institute of the Blind.

If you need more advice ask your pharmacist.

BTC 23038 vD 28/03/08


Download




Family Meltus Chesty Coughs Honey & Lemon Flavour


1. Name Of The Medicinal Product

Family Meltus Chesty Coughs Honey and Lemon Flavour

2. Qualitative And Quantitative Composition

Guaifenesin BP 50.00mg/5ml.

3. Pharmaceutical Form

Syrup.

4. Clinical Particulars 4.1 Therapeutic Indications

Symptomatic relief of deep chesty coughs and to soothe the throat.

4.2 Posology And Method Of Administration

Route of administration: Oral. To be taken three or four times daily.

Adults and children over 12 years: Two to four 5ml spoonfuls.

Children 6–12 years: Two 5ml spoonfuls.

Children 2-6 years: One 5ml spoonful.

Children under 2 years: On medical advice only.

4.3 Contraindications

None known.

4.4 Special Warnings And Precautions For Use

None.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

None known.

4.6 Pregnancy And Lactation

May be used.

4.7 Effects On Ability To Drive And Use Machines

None known.

4.8 Undesirable Effects

Some gastrointestinal discomfort has been reported.

4.9 Overdose

Very large doses may cause nausea and vomiting. The drug is, however, rapidly metabolised and excreted in the urine. Treatment: The patient should be kept under observation and treated symptomatically.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

Guaifenesin is an expectorant. The sugar, honey and glycerin have a demulcent effect.

5.2 Pharmacokinetic Properties

Guaifenesin is absorbed from the gastrointestinal tract. It is metabolised and excreted in the urine.

5.3 Preclinical Safety Data

There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Purified Honey BP; Sunset Yellow E110; Sucrose, Granular BP; Glycerin BP; Tolu Flavour Solution–Sugar Free HSE; Sodium Benzoate BP; Citric Acid Monohydrate BP; Lemon Oil Terpeneless BP; Isopropyl Alcohol BP; Sodium Cyclamate Ph Eur; Purified Water USP.

6.2 Incompatibilities

Not applicable.

6.3 Shelf Life

Three years.

6.4 Special Precautions For Storage

Store below 20oC.

6.5 Nature And Contents Of Container

Amber glass sirop bottles fitted with a tamper evident cap with fitted polycone liner packed in an outer carton containing 100ml of product.

6.6 Special Precautions For Disposal And Other Handling

Not applicable.

7. Marketing Authorisation Holder

Cupal Ltd. Venus, 1 Old Park Lane, Trafford Park, Manchester M41 7HA

8. Marketing Authorisation Number(S)

PL 0338/0064.

9. Date Of First Authorisation/Renewal Of The Authorisation

17th November 1987 /26th February 2004.

10. Date Of Revision Of The Text

August 2006


Download




Adult Meltus for Chesty Coughs and Catarrh


1. Name Of The Medicinal Product

Adult Meltus for Chesty Coughs and Catarrh.

2. Qualitative And Quantitative Composition

Guaifenesin 100mg / 5ml

Cetylpyridinium Chloride 2.5mg / 5ml

Sucrose 1.75g / 5ml

Purified Honey 0.5g / 5ml

3. Pharmaceutical Form

Oral liquid

4. Clinical Particulars 4.1 Therapeutic Indications

For the symptomatic relief of coughs and catarrh associated with influenza, colds and mild throat infections.

4.2 Posology And Method Of Administration

Oral.

Adults and children over 12 years:

One or two 5ml spoonfuls to be taken and swallowed slowly every three or four hours. Not recommended for children under 12 years.

4.3 Contraindications

No known contraindications.

4.4 Special Warnings And Precautions For Use

Not suitable for children under 12 years.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

Can cause transient abnormality in platelet aggregation patterns determined one hour after ingestion.

4.6 Pregnancy And Lactation

No known contraindications.

4.7 Effects On Ability To Drive And Use Machines

None known.

4.8 Undesirable Effects

Some gastrointestinal discomfort. Very large doses may cause nausea and vomiting.

4.9 Overdose

Very large doses may cause nausea and vomiting, it is however rapidly metabolised and excreted in the urine. The patient should be kept under observation and treated symptomatically.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

A cough linctus containing an expectorant and an oral antiseptic in a honey and syrup demulcent base. The expectorant, guaifenesin, is employed to produce a thinning of mucous secretions and thus gives relief in bronchial catarrh. The antiseptic, cetylpyridinium chloride, is used for the treatment of superficial mouth and throat infections.

5.2 Pharmacokinetic Properties

None stated.

5.3 Preclinical Safety Data

None stated.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Glycerin

Alcohol (96%)

Aniseed oil

Menthol crystals

Chloroform

Caramel (E150)

Glucose Liquid

Purified Water

6.2 Incompatibilities

None known.

6.3 Shelf Life

Five years.

6.4 Special Precautions For Storage

Store below 25oC.

6.5 Nature And Contents Of Container

Glass amber sirop bottle with tamper evident cap with fitted ploycone liner in an individual carton containing 100ml or 200 ml of product, including a 5ml CE marked polystyrene measuring spoon.

6.6 Special Precautions For Disposal And Other Handling

No special requirements

7. Marketing Authorisation Holder

Cupal Limited, Venus, 1 Old Park Lane, Trafford Park, Manchester, M41 7HA

8. Marketing Authorisation Number(S)

PL 0338/5026R

9. Date Of First Authorisation/Renewal Of The Authorisation

14/09/90 / 07/09/99

10. Date Of Revision Of The Text

July 2006


Download




Expectorants


A drug may be classified by the chemical type of the active ingredient or by the way it is used to treat a particular condition. Each drug can be classified into one or more drug classes.

Expectorants are drugs that increase the bronchial secretion and enhance the expulsion of mucus by air passages of the lungs. This makes it is easier to cough up the phlegm or sputum. Expectorants are used in cough mixtures for chesty coughs.

See also

Medical conditions associated with expectorants:

Bronchitis Cough Cutaneous Sporotrichosis Fibromyalgia Hyperthyroidism Radiation Emergency Drug List: Duratuss-G Pima-Syrup Mucinex Guaifenesin-La Altarussin Amibid-La Availnex-Chewable-Tablets Benylin-E-Extra-Strength-Chest-Congestion Bidex-400 Drituss-G Ganidin-Nr Gg-200-Nr Guaifenex-G Guaifenex-La Guaituss-Liquid Hytuss-Immediate-Release-Capsules Iosat Liquibid Mucinex-Children-S-Granules Muco-Fen-1200 Organidin-Nr-Immediate-Release-Capsules Q-Bid-La Robitussin Scot-Tussin Sski-Drops Thyroshield-Solution Diabetic-Tussin-Ex Yodefan-Liquid Yodefan-Nf


Download




Beechams Veno’s Cough Mixture


1. Name Of The Medicinal Product

Beechams Veno's Cough Mixture

Veno's Cough Syrup

2. Qualitative And Quantitative Composition

Glucose liquid 3.18 g, Treacle 1.35 g

For excipients, see 6.1.

3. Pharmaceutical Form

Syrup

4. Clinical Particulars 4.1 Therapeutic Indications

Recommended for the symptomatic relief of sore throat and unproductive cough in minor respiratory tract infections.

4.2 Posology And Method Of Administration

Adults and children over the age of 12: Take one 5 ml or 10 ml dose (one or two 5 ml spoonfuls). Repeat the dose every 2 or 3 hours.

Children aged 3 to under 12 years: Take one 5 ml dose (one 5 ml spoonful) and give every 2 to 3 hours. Do not give to children under 3 years except on medical advice.

Route of Administration

Oral

4.3 Contraindications

Hypersensitivity to glucose, treacle or any other of the ingredients.

4.4 Special Warnings And Precautions For Use

Special Label Warnings

Keep all medicines out of the sight and reach of children.

If symptoms persist consult your doctor.

Total sugars content 3.6 g per 5 ml.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

None

4.6 Pregnancy And Lactation

Use in pregnancy and lactation is not contraindicated. However, as with all medicines, caution should be exercised during pregnancy and lactation.

4.7 Effects On Ability To Drive And Use Machines

None

4.8 Undesirable Effects

Immune system disorders

Hypersensitivity reactions e.g. skin rash

4.9 Overdose

The product does not contain any ingredient in a high enough concentration to cause toxic effects; therefore no specific symptoms of overdosage would be anticipated and no antidotes would be required.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

Treacle and glucose liquid are demulcents, which will help relieve an unproductive cough and will soothe a sore throat.

5.2 Pharmacokinetic Properties

None Stated.

5.3 Preclinical Safety Data

There are no preclinical data of any relevance additional to that already included in other sections of the SmPC.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Capsicum tincture, aniseed oil, xanthan gum, camphor racemic, glacial acetic acid, sodium benzoate, sodium metabisulphite (E223), levomenthol, water and colour caramel (E150).

6.2 Incompatibilities

None

6.3 Shelf Life

Unopened: Three years

Opened: Six months

6.4 Special Precautions For Storage

None

6.5 Nature And Contents Of Container

Clear glass bottle with a roll-on, pilfer proof, aluminium cap containing a melinex-coated aluminium-faced pulp-board wad. The bottle is contained in a boxboard carton.

Pack sizes: 100 ml, 160 ml.

Not all pack sizes may be marketed.

6.6 Special Precautions For Disposal And Other Handling

None

Administrative Data 7. Marketing Authorisation Holder

Beecham Group plc

980 Great West Road

Brentford

Middlesex

TW8 9GS

United Kingdom

Trading as:

GlaxoSmithKline Consumer Healthcare, Brentford, TW8 9GS, U.K.

8. Marketing Authorisation Number(S)

PL 00079/0157R

9. Date Of First Authorisation/Renewal Of The Authorisation

28 September 1988 / 9 November 1993

10. Date Of Revision Of The Text

01/12/2010


Download




Boots Catarrh Pastilles


Boots Catarrh Pastilles

(Eucalyptus Oil, Menthol, Pumilio Pine Oil)

relieves catarrh, coughs and colds

45 g

Read all of this carton for full instructions.

What this medicine is for

This medicine contains menthol, eucalyptus and pumilio oils, which relieve chesty coughs and have antiseptic properties. It can be used to relieve the symptoms of congestion caused by catarrh, coughs and colds.

Before you take this medicine Do not take: If you are allergic to any of the ingredients If you have an intolerance to some sugars, unless your doctor tells you to (this medicine contains glucose and sucrose) Talk to your pharmacist or doctor: If you are pregnant or breastfeeding

Information about some of the ingredients: Each pastille contains a total of 0.8 g of glucose and sucrose. This should be taken into account by people with diabetes. The colour E122 in this medicine may cause allergic reactions.

How to take this medicine

Check the inner bag is not broken before use. If it is, do not use the pastilles.

Adults and children of 12 years and over: Suck one pastille when you need to.

Don’t take more than 20 pastilles in 24 hours.

Suck each pastille slowly until it dissolves.

Do not give to children under 12 years.

Do not take more than the amount recommended.

If symptoms do not go away, talk to your doctor.

If you take too many pastilles: Talk to a pharmacist or doctor straight away.

Possible side effects

Most people will not have problems, but some may get some.

If you get any of these serious side effects, stop taking the pastilles. See a doctor at once:

Difficulty in breathing, swelling of the face, neck, tongue or throat (severe allergic reactions)

If any side effect becomes severe, or you notice any side effect not listed here, please tell your pharmacist or doctor.

How to store this medicine

Do not store above 25°C.

Keep all medicines out of the sight and reach of children.

Use by the date on the end flap of the carton.

Active ingredients

Each pastille contains Eucalyptus Oil 0.02% v/w, Menthol 0.8% w/w, Pumilio Pine Oil 0.6% v/w.

Also contains: modified starch, sucrose, glucose syrup, marshmallow liquid extract, vegetable oil, beeswax, water, thymol, carmoisine (E122).

PL 00094/0009

Text prepared 8/09

Manufactured for

The Boots Company PLC Nottingham NG2 3AA

by The Marketing Authorisation holder

Ernest Jackson and Co Crediton Devon EX17 3AP

If you need more advice ask your pharmacist.


Download




Heliox



Dosage Form: gas
COMPRESSED GAS N.O.S. (HELIUM, OXYGEN 20) LABEL

COMPRESSED GAS, N.O.S. (HELIUM, OXYGEN) NON-FLAMMABLE GAS 2 UN 1956

MEDICAL GAS MIXTURE   BALANCE HELIUM, USP  CAS:   7440-59-7  20.0%OXYGEN, USP   CAS:   7782-44-7

CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. RX ONLY.

WARNING: HIGH PRESSURE GAS. MAY ACCELERATE COMBUSTION.

KEEP OIL AND GREASE AWAY. USE ONLY USE WITH EQUIPMENT CLEANED FOR OXYGEN SERVICE AND RATED FOR CYLINDER PRESSURE. USE EQUIPMENT RATED FOR CYLINDER PRESSURE. STORE AND USE WITH ADEQUATE VENTILATION. CLOSE VALVE AFTER EACH USE AND WHEN EMPTY. OPEN VALVE SLOWLY. ADMINISTRATION OF THIS GAS MIXTURE MAY BE HAZARDOUS OR CONTRAINDICATED. FOR USE ONLY BY OR UNDER THE SUPERVISION OF A LICENSED PRACTITIONER WHO IS EXPERIENCED IN THE USE AND ADMINISTRATION OF GAS MIXTURES AND IS FAMILIAR WITH THE INDICATIONS, EFFECTS, DOSAGES, METHODS, AND FREQUENCY AND DURATION OF ADMINISTRATION, AND WITH THE HAZARDS, CONTRAINDICATIONS AND SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN. USE IN ACCORDANCE WITH THE APPROPRIATE MSDS FOR EACH MIXTURE COMPONENT. SECURE CYLINDER WHILE IN TRANSPORTATION, STORAGE AND IN USE.

FIRST AID: IF INHALED, REMOVE TO FRESH AIR. IF NOT BREATHING, GIVE ARTIFICIAL RESPIRATION. IF BREATHING IS DIFFICULT, GIVE OXYGEN. CALL A PHYSICIAN.

SERIAL NUMBER:  0000000   LOT NO:  0000000 - VOLUME: 204.1 - EXP. DATE: 1/1/2015 VER. 3.11

FOR MEDICAL USE ONLY   DO NOT REMOVE THIS PRODUCT LABEL

COMPRESSED GAS N.O.S. (HELIUM, OXYGEN 25) LABEL

COMPRESSED GAS, OXIDIZING, N.O.S. (OXYGEN, HELIUM) NON-FLAMMABLE GAS 2 OXIDIZER 5.1 UN 3156

MEDICAL GAS MIXTURE  25.0% OXYGEN USP   CAS:  7782-44-7  BALANCE HELIUM, USP   CAS:   7440-59-7

CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. RX ONLY.

WARNING: OXIDIZING HIGH PRESSURE GAS. VIGOROUSLY ACCELERATES COMBUSTION.

KEEP OIL AND GREASE AWAY. USE ONLY USE WITH EQUIPMENT CLEANED FOR OXYGEN SERVICE AND RATED FOR CYLINDER PRESSURE. USE EQUIPMENT RATED FOR CYLINDER PRESSURE. STORE AND USE WITH ADEQUATE VENTILATION. CLOSE VALVE AFTER EACH USE AND WHEN EMPTY. OPEN VALVE SLOWLY. ADMINISTRATION OF THIS GAS MIXTURE MAY BE HAZARDOUS OR CONTRAINDICATED. FOR USE ONLY BY OR UNDER THE SUPERVISION OF A LICENSED PRACTITIONER WHO IS EXPERIENCED IN THE USE AND ADMINISTRATION OF GAS MIXTURES AND IS FAMILIAR WITH THE INDICATIONS, EFFECTS, DOSAGES, METHODS, AND FREQUENCY AND DURATION OF ADMINISTRATION, AND WITH THE HAZARDS, CONTRAINDICATIONS AND SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN. USE IN ACCORDANCE WITH THE APPROPRIATE MSDS FOR EACH MIXTURE COMPONENT. SECURE CYLINDER WHILE IN TRANSPORTATION, STORAGE AND IN USE.
FIRST AID: IF INHALED, REMOVE TO FRESH AIR. IF NOT BREATHING, GIVE ARTIFICIAL RESPIRATION. IF BREATHING IS DIFFICULT, GIVE OXYGEN. CALL A PHYSICIAN.
SERIAL NUMBER: 0000000   LOT NO:0000000 - VOLUME: 200 - EXP. DATE: 1/1/2015 VER. 3.11
FOR MEDICAL USE ONLY. DO NOT REMOVE THIS PRODUCT LABEL.

COMPRESSED GAS N.O.S. (HELIUM, OXYGEN 30) LABEL

COMPRESSED GAS, OXIDIZING, N.O.S. (HELIUM, OXYGEN) NON-FLAMMABLE GAS 2  OXIDIZER 5.1  UN 3156

MEDICAL GAS MIXTURE  BALANCE HELIUM, USP   CAS:   7440-59-7  30.0% OXYGEN, USP   CAS:   7782-44-7

CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. RX ONLY.

WARNING: OXIDIZING HIGH PRESSURE GAS. VIGOROUSLY ACCELERATES COMBUSTION.

KEEP OIL AND GREASE AWAY. USE ONLY USE WITH EQUIPMENT CLEANED FOR OXYGEN SERVICE AND RATED FOR CYLINDER PRESSURE. USE EQUIPMENT RATED FOR CYLINDER PRESSURE. STORE AND USE WITH ADEQUATE VENTILATION. CLOSE VALVE AFTER EACH USE AND WHEN EMPTY. OPEN VALVE SLOWLY. ADMINISTRATION OF THIS GAS MIXTURE MAY BE HAZARDOUS OR CONTRAINDICATED. FOR USE ONLY BY OR UNDER THE SUPERVISION OF A LICENSED PRACTITIONER WHO IS EXPERIENCED IN THE USE AND ADMINISTRATION OF GAS MIXTURES AND IS FAMILIAR WITH THE INDICATIONS, EFFECTS, DOSAGES, METHODS, AND FREQUENCY AND DURATION OF ADMINISTRATION, AND WITH THE HAZARDS, CONTRAINDICATIONS AND SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN. USE IN ACCORDANCE WITH THE APPROPRIATE MSDS FOR EACH MIXTURE COMPONENT. SECURE CYLINDER WHILE IN TRANSPORTATION, STORAGE AND IN USE.
FIRST AID: IF INHALED, REMOVE TO FRESH AIR. IF NOT BREATHING, GIVE ARTIFICIAL RESPIRATION. IF BREATHING IS DIFFICULT, GIVE OXYGEN. CALL A PHYSICIAN.
SERIAL NUMBER:  00000000   LOT NO.:0000000 - VOLUME: 204.1 - EXP. DATE: 1/1/2013 VER. 3.11
FOR MEDICAL USE ONLY.  DO NOT REMOVE THIS PRODUCT LABEL.







Heliox 
Heliox  gas Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 10006-009 Route of Administration RESPIRATORY (INHALATION) DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYGEN (OXYGEN) OXYGEN 20 L  in 100 L Inactive Ingredients Ingredient Name Strength HELIUM 80 L  in 100 L Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 10006-009-01 6032 L In 1 CYLINDER None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved medical gas 01/01/1936
Heliox 
Heliox  gas Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 10006-010 Route of Administration RESPIRATORY (INHALATION) DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYGEN (OXYGEN) OXYGEN 25 L  in 100 L Inactive Ingredients Ingredient Name Strength HELIUM 75 L  in 100 L Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 10006-010-01 6032 L In 1 CYLINDER None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved medical gas 01/01/1936
Heliox 
Heliox  gas Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 10006-011 Route of Administration RESPIRATORY (INHALATION) DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYGEN (OXYGEN) OXYGEN 30 L  in 100 L Inactive Ingredients Ingredient Name Strength HELIUM 70 L  in 100 L Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 10006-011-01 6032 L In 1 CYLINDER None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved medical gas 01/01/1936
Labeler - Acetylene Oxygen Company (008110181) Registrant - Acetylene Oxygen Company (008110181) Establishment Name Address ID/FEI Operations Acetylene Oxygen Company 809889033 manufacture Revised: 04/2011Acetylene Oxygen Company
More Heliox resources Heliox Drug Interactions Heliox Support Group 0 Reviews · Be the first to review/rate this drug


Download




Carbon Dioxide Oxygen Mixture


Dosage Form: gas
Carbon Dioxide Oxygen Mixture

COMPRESSED GAS, OXIDIZING, N.O.S.
(  % CARBON DIOXIDE USP,    %OXYGEN USP) UN 3156 NON-FLAMMABLE 2    OXIDIZER 5.1   30460D (06/02)
OXYGEN CONTENT OVER 23.5% Rx only. CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. WARNING: Administration of this gas may be hazardous or contraindicated. For use only by under the supervision of a licensed practitioner who is experienced in the use and administration of gas mixtures and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindication and side effects, and the precautions to be taken. CAUTION: HIGH PRESSURE OXIDIZING GAS. VIGOROUSLY ACCELERATES COMBUSTION. MIXTURES CONTAINING CARBON DIOXIDE CAN INCREASE RESPIRATION AND HEART RATE. Keep oil and grease away. Open valve slowly. Store and use with adequate ventilation. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Cylinder temperature should not exceed 52C (125F). Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.  CARBON DIOXIDE CAS: 124-38-9 OXYGEN CAS: 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.
FILLED and INSPECTED BY GENERAL AIR SERVICE and SUPPLY DENVER, CO 80204

COMPRESSED GAS, OXIDIZING, N.O.S.
(  % CARBON DIOXIDE USP,    %OXYGEN USP) UN 3156 NON-FLAMMABLE 2    OXIDIZER 5.1   30460D (06/02)
OXYGEN CONTENT OVER 23.5% Rx only. CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. WARNING: Administration of this gas may be hazardous or contraindicated. For use only by under the supervision of a licensed practitioner who is experienced in the use and administration of gas mixtures and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindication and side effects, and the precautions to be taken. CAUTION: HIGH PRESSURE OXIDIZING GAS. VIGOROUSLY ACCELERATES COMBUSTION. MIXTURES CONTAINING CARBON DIOXIDE CAN INCREASE RESPIRATION AND HEART RATE. Keep oil and grease away. Open valve slowly. Store and use with adequate ventilation. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Cylinder temperature should not exceed 52C (125F). Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.  CARBON DIOXIDE CAS: 124-38-9 OXYGEN CAS: 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.
FILLED and INSPECTED BY GENERAL AIR SERVICE and SUPPLY DENVER, CO 80204


Carbon Dioxide Oxygen Mixture 
Carbon Dioxide Oxygen Mixture  gas Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 21220-129 Route of Administration RESPIRATORY (INHALATION) DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Carbon Dioxide (Carbon Dioxide) Carbon Dioxide 200 mL  in 1 L Oxygen (Oxygen) Oxygen 800 mL  in 1 L Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 21220-129-01 7101 L In 1 CYLINDER None 2 21220-129-02 707 L In 1 CYLINDER None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved medical gas 01/01/1975
Labeler - General Air Service & Supply Co (151227338) Establishment Name Address ID/FEI Operations General Air Service & Supply Co 006686091 manufacture Revised: 10/2010General Air Service & Supply Co


Download




Magnesium Trisilicate Mixture BP


1. Name Of The Medicinal Product

Magnesium Trisilicate Mixture BP or Indigestion Mixture.

2. Qualitative And Quantitative Composition

Magnesium carbonate light

250mg/5ml

Magnesium trisilicate

250mg/5ml

Sodium hydrogen carbonate

250mg/5ml

For full list of excipients see section 6.1

3. Pharmaceutical Form

Mixture

4. Clinical Particulars 4.1 Therapeutic Indications

For relief of the symptoms of indigestion, heartburn and dyspepsia.

4.2 Posology And Method Of Administration

Oral.

RECOMMENDED DOSE

Adults and children over 12 years: two to four 5ml spoonfuls.

Children 5 to 12 years: one to two 5ml spoonfuls.

Directions for use: shake the bottle.

Take in a little water.

DOSAGE SCHEDULE

To be taken three times a day or as required.

4.3 Contraindications

Contraindicated in severe renal failure and hypophosphataemia.

Should not be administered to patients with metabolic or respiratory alkalosis, hypocalcaemia or hypochlorhydria.

Hypersensitivity to any of the ingredients.

4.4 Special Warnings And Precautions For Use

The product should be used with caution in patients with fluid retention. In view of the sodium hydrogen carbonate content the product should also be administered extremely cautiously to patients with congestive heart failure, renal impairment, cirrhosis of the liver, hypertension and to patients receiving corticosteroids.

If renal function is impaired hypermagnesaemia may result giving the symptoms described under (9) overdose.

The following warnings and precautions appear on the labels:

Keep all medicines away from children

Discard any unused mixture one month after opening.

If symptoms persist consult your doctor.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

Antacids may interact with a number of other drugs by altering their absorption and, sometimes, their elimination. Examples include diflunisal, phenytoin, cimetidine, mexiletine, chlorpromazine, isoniazid, allopurinol, iron preparations, tetracyclines, phenothiazines, penicillamine, pivampicillin, atenolol, diclofenac, digitoxin, ibuprofen, indomethacin, ketoprofen, levodopa, metoprolol, metronidazole, ketoconazole, itraconazole, prednisolone, quinidine, tolfenamic acid, ciprofloxacin, ofloxacin, norfloxacin, rifampicin, azithromycin aspirin, fosinopril, dipyridamole, hydroxychloroquine, chloroquine, diazepam, bisphosphonates, warfarin and lithium.

4.6 Pregnancy And Lactation

Animal studies are insufficient with respect to effects on pregnancy, embryonal/foetal development, parturition and postnatal development (see section 5.3). The potential risk for humans is unknown.

Caution should be exercised when prescribing to pregnant women.

4.7 Effects On Ability To Drive And Use Machines

None.

4.8 Undesirable Effects

Magnesium salts may cause diarrhoea in some patients. Magnesium carbonate and sodium hydrogen carbonate may cause stomach cramps and flatulence as a result of excess carbon dioxide production.

4.9 Overdose

Overdose, or excessive or prolonged intake of magnesium containing antacids may give rise to hypermagnesaemia, and excessive administration of sodium hydrogen carbonate may lead to hypokalaemia and metabolic alkalosis, especially in patients with renal insufficiency.

Symptoms of hypermagnesaemia include nausea, vomiting, flushing of the skin, thirst, drowsiness, hypotension, confusion, muscle weakness, CNS and respiratory depression, hyporeflexia, peripheral vasodilatation, bradycardia, cardiac arrhythmias, coma and cardiac arrest. Treatment of mild hypermagnesaemia is usually limited to restricting magnesium intake. In severe hypermagnesaemia, ventilatory and circulatory support may be required.

Treatment should consist of the intravenous administration of calcium gluconate injection 100% at a dose of 10 – 20ml, to counteract respiratory depression or heart block. If renal function is normal, adequate fluids should be given to assist magnesium removal from the body. Haemodialysis may be necessary in patients with renal impairment or for whom other methods prove ineffective. Metabolic alkalosis and hypernatraemia can be treated by appropriate correction of fluid and electrolyte balance.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

Magnesium trisilicate mixture is an antacid with slow neutralising action and mild laxative action.

5.2 Pharmacokinetic Properties

Magnesium chloride and hydrated silica gel are formed during the neutralisation. About 5% of magnesium is absorbed and traces of liberated silica may be absorbed and excreted in the urine.

Any sodium hydrogen carbonate not neutralised in the stomach is absorbed and excreted as bicarbonate and sodium ions in the urine in the absence of a plasma deficit.

5.3 Preclinical Safety Data

None known.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Sodium nipasept, peppermint oil, chloroform, polysorbate 20, purified water.

6.2 Incompatibilities

None.

6.3 Shelf Life

200ml: 18 months unopened, 1 month after first opening.

500ml: 18 months unopened, 1 month after first opening.

6.4 Special Precautions For Storage

Store below 25°C.

6.5 Nature And Contents Of Container

200ml: amber glass bottle with polypropylene cap or white 28mm cap with tamper evident band and EPE/Saranex liner.

500ml: amber glass bottle with plastic lined cap or white 28mm cap with tamper evident band and EPE/Saranex liner.

6.6 Special Precautions For Disposal And Other Handling

None.

7. Marketing Authorisation Holder

L.C.M. Ltd

Linthwaite laboratories

Huddersfield

HD7 5QH

8. Marketing Authorisation Number(S)

PL 12965/0025

9. Date Of First Authorisation/Renewal Of The Authorisation

10th May 1994 / 10th May 1999

10. Date Of Revision Of The Text

10/10/2011


Download




Vicks Cough Lozenges with Honey


Vicks Cough Lozenges with Honey

Dextromethorphan 7.33mg per Lozenge

In this leaflet: 1. What Vicks Cough Lozenges with Honey are and what they are used for 2. Before you take Vicks Cough Lozenges with Honey 3. How to take Vicks Cough Lozenges with Honey 4. Possible side effects 5. How to store Vicks Cough Lozenges with Honey 6. Further information Read all of this leaflet carefully because it contains important information for you.

This medicine is available without prescription. However, you still need to take Vicks Cough Lozenges with Honey carefully to get the best results from them.

Keep this leaflet. You may need to read it again. Ask your pharmacist if you need more information or advice. You must contact a doctor if your symptoms worsen or do not improve. If any of the side effects become serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist. What Vicks Cough Lozenges with Honey are and what they are used for

Vicks Cough Lozenges with Honey contain the active ingredient Dextromethorphan which suppresses a cough by acting on the cough centre of the brain. These lozenges relieve dry coughs associated with colds and flu.

Before you take Vicks Cough Lozenges with Honey Do not take Vicks Cough Lozenges with Honey if you: are allergic to dextromethorphan or other ingredients (see section 6) have severe liver disease have a productive cough - (coughing produces mucus/phlegm). are taking medicines called monoamine oxidase inhibitors (MAOIs – a type of antidepressant) or have taken them in the last 14 days.

Do not give Vicks cough lozenges with honey to children under 12 years of age.

Take special care with Vicks Cough Lozenges with Honey

Talk to your doctor or pharmacist before taking this medicine if you:

have asthma you have ever had liver problems are diabetic or have difficulty digesting some sugars you have any long standing problems with your lungs Taking other medicines

Do not take Vicks Cough Lozenges with Honey if you are taking medicine
for depression or Parkinson’s disease called monoamine oxidase inhibitors (MAOIs) or have done so in the last 14 days.

Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking this product if you are pregnant or breast feeding.

Driving and using machines

If you feel dizzy, experience confusion or have symptoms of excitation (rapid pulse, hyperactivity or excessive sweating) do not drive or operate machinery.

Important information about some of the ingredients of Vicks Cough Lozenges with Honey:

Each lozenge contains 3.3g of sugar (as sucrose and glucose syrup). This should be taken into account if you are diabetic. If you have been told by your doctor that you have an intolerance to some sugars, consult your doctor before taking this medicinal product.

How to take Vicks Cough Lozenges with Honey

Always use Vicks Cough Lozenges with Honey exactly as your doctor or pharmacist has told you. You should check with your doctor or pharmacist if you are not sure.

Dosage

Adults and children over 12 years : 2 lozenges, sucked one after the other.

Repeat the dose every 6 hours if required. Do not take more than 8 lozenges in 24 hours.

Do not give this medicine to children under 12 years of age.

Do not exceed the recommended dose.

If symptoms persist, speak to your pharmacist or doctor.

If you take more Vicks Cough Lozenges with Honey than you should

Seek medical advice immediately if you accidentally take more lozenges than you should.

If you forget to take Vicks Cough Lozenges with Honey

If you accidentally miss a dose, do not take a double dose; just take the next dose as normal.

Possible side effects

Like all medicines, Vicks Cough Lozenges with Honey can cause side effects, although not everyone gets them.

These may include: Dizziness Excitation (rapid pulse, hyperactivity or excessive sweating). Mental confusion Stomach upsets

If any side effects you experience become serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

How to store Vicks Cough Lozenges with Honey

Keep out of the reach and sight of children.

Store below 25°C. Store in original packaging.

Do not take Vicks Cough Lozenges with Honey after the expiry date which is printed on the carton.

The expiry date refers to the last day of the month stated.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

Further information What Vicks Cough Lozenges with Honey contain:

Active ingredient: 7.33 mg Dextromethorphan base per lozenge. Other ingredients: Sucrose, glucose syrup, honey, levomenthol, honey flavour, caramel flavour.

This pack contains 12 lozenges in a blister foil.

Marketing Authorisation Holder Procter & Gamble (Health & Beauty Care) Limited Weybridge Surrey KT13 0XP UK

(send all enquiries to this address).

Manufacturer: Procter & Gamble Manufacturing GmbH Procter & Gamble Strasse 1 64521, Gross Gerau Germany

PL 0129/0129

Text Revised: 04/2009

98873922


Download




ElixSure Cough Gel Syrup


Pronunciation: DEX-troe-meth-OR-fan
Generic Name: Dextromethorphan
Brand Name: ElixSure Cough
ElixSure Cough Gel Syrup is used for:

Temporarily relieving cough due to the common cold, hay fever, upper respiratory tract infections, sinus inflammation, sore throat, or bronchitis.

ElixSure Cough Gel Syrup is a cough suppressant. It works in the cough center of the brain to reduce a dry or nonproductive cough.

Do NOT use ElixSure Cough Gel Syrup if: you are allergic to any ingredient in ElixSure Cough Gel Syrup you are taking or have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using ElixSure Cough Gel Syrup:

Some medical conditions may interact with ElixSure Cough Gel Syrup. Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, plan to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have chronic cough, chronic bronchitis, asthma, emphysema, chronic obstructive pulmonary disease (COPD), or if cough occurs with a large amount of mucus

Some MEDICINES MAY INTERACT with ElixSure Cough Gel Syrup. Tell your health care provider if you are taking any other medicines, especially any of the following:

Furazolidone or MAO inhibitors (eg, phenelzine) because the risk of toxic side effects may be increased by ElixSure Cough Gel Syrup

This may not be a complete list of all interactions that may occur. Ask your health care provider if ElixSure Cough Gel Syrup may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use ElixSure Cough Gel Syrup:

Use ElixSure Cough Gel Syrup as directed by your doctor. Check the label on the medicine for exact dosing instructions.

ElixSure Cough Gel Syrup may be taken with or without food. Take with food if stomach upset occurs. Shake well before using. Use the teaspoon provided with ElixSure Cough Gel Syrup to measure your dose. Ask your pharmacist for help if you are unsure of how to measure your dose. If you miss a dose of ElixSure Cough Gel Syrup and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use ElixSure Cough Gel Syrup.

Important safety information: ElixSure Cough Gel Syrup may cause drowsiness, dizziness, blurred vision, or lightheadedness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to ElixSure Cough Gel Syrup. Using ElixSure Cough Gel Syrup alone, with certain other medicines, or with alcohol may lessen your ability to drive or to perform other potentially dangerous tasks. If your cough lasts for more than 1 week or comes back, or if you also have a fever, rash, or persistent headache, contact your health care provider. A persistent cough could be a sign of a serious condition. ElixSure Cough Gel Syrup contains dextromethorphan. Before you being taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains dextromethorphan. If it does or if you are not sure, contact your health care provider or pharmacist. Diabetes patients - Some brands of ElixSure Cough Gel Syrup may contain sugar and affect your blood sugar level. Read the label carefully before using ElixSure Cough Gel Syrup. ElixSure Cough Gel Syrup is not recommended for use in CHILDREN younger than 2 years of age. Safety and effectiveness in this age group have not been confirmed. PREGNANCY and BREAST-FEEDING: It is unknown if ElixSure Cough Gel Syrup can cause harm to the fetus. If you become pregnant while taking ElixSure Cough Gel Syrup, discuss with your doctor the benefits and risks of using ElixSure Cough Gel Syrup during pregnancy. It is unknown if ElixSure Cough Gel Syrup is excreted in breast milk. Do not breast-feed while taking ElixSure Cough Gel Syrup. Possible side effects of ElixSure Cough Gel Syrup:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; drowsiness; stomach upset.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: ElixSure Cough side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include confusion; excitement; hallucinations; slowed breathing.

Proper storage of ElixSure Cough Gel Syrup:

Store ElixSure Cough Gel Syrup between 68 and 77 degrees F (20 and 25 degrees C), away from heat, moisture, and light. Do not store in the bathroom. Keep ElixSure Cough Gel Syrup out of the reach of children and away from pets.

General information: If you have any questions about ElixSure Cough Gel Syrup, please talk with your doctor, pharmacist, or other health care provider. ElixSure Cough Gel Syrup is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about ElixSure Cough Gel Syrup. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More ElixSure Cough resources ElixSure Cough Side Effects (in more detail) ElixSure Cough Use in Pregnancy & Breastfeeding ElixSure Cough Drug Interactions ElixSure Cough Support Group 0 Reviews for ElixSure Cough - Add your own review/rating Compare ElixSure Cough with other medications Cough


Download




Scot-Tussin Expectorant SF Cough


guaifenesin
Dosage Form: oral liquid
Scot-Tussin Expectorant SF Cough Active Ingredient: 

Each teaspoonful (5 ml) contains:

Guaifenesin 100mg

Purpose

Expectorant

Uses Helps loosen phlegm (mucus) to make coughs more productive thereby relieving chest congestion. Warnings Do not exceed recommended dosage.
*Phenylketonurics: Contains Phenylalanine. When using this product Do not exceed recommended dosage. Ask a doctor before use if you have a Cough that occurs with too much phlegm (mucus).
a Chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema. Stop use and ask a doctor if Cough lasts more than seven days, returns or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. If pregnant or breast-feeding,

Do Not Use.

Keep out of reach of children.

In case of overdose get medical help or contact a Poison Control Center right away.

Directions: Follow Dosage Chart.
Do not exceed six doses in any 24 hour period. Adults 2-4 teaspoonfuls (10-20 ml)
every 4 hours Children 12 years
and older Consult a Doctor Children Under
12 years old DO NOT USE Other Information Store at 20? – 25? C (68? – 77? F). Inactive Ingredients

Aspartame* (see warning) Benzoic Acid, Citric Acid, Clear Grape Flavor, Glycerin, Hydroxypropylmethylcellulose, Menthol, Methyl-Paraben, Propyl-Paraben, Propylene Glycol, Purified Water, *Phenylketonurics: Contains Phenylalanine.

PRINCIPAL DISPLAY PANEL

NDC 0372-0006-04

SCOT-TUSSIN

EXPECTORANT

COUGH

For DIABETICS since 1956

SUGAR-FREE

LOOSENS &

RELIEVES

CHEST

CONGESTION

100%

SUGAR-FREE
HIGH BLOOD PRESSURE SAFE
LACTOSE-FREE
ALCOHOL-FREE
SODIUM-FREE
CLEAR
GLUTEN-FREE

Scot-Tussin

STRIVING FOR PERFECTION

4 FL OZ (118 ml)


Scot-Tussin Expectorant SF Cough 
guaifenesin  liquid Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0372-0006 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 100 mg  in 5 mL Inactive Ingredients Ingredient Name Strength ASPARTAME   BENZOIC ACID   CITRIC ACID MONOHYDRATE   GLYCERIN   HYPROMELLOSE   MENTHOL   METHYLPARABEN   PROPYLPARABEN   PROPYLENE GLYCOL   WATER   Product Characteristics Color      Score      Shape Size Flavor GRAPE Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 0372-0006-04 118 mL In 1 BOTTLE None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part341 07/01/1974
Labeler - SCOT-TUSSIN Pharmacal Co., Inc. (001203918) Revised: 04/2009SCOT-TUSSIN Pharmacal Co., Inc.
More Scot-Tussin Expectorant SF Cough resources Scot-Tussin Expectorant SF Cough Side Effects (in more detail) Scot-Tussin Expectorant SF Cough Dosage Scot-Tussin Expectorant SF Cough Use in Pregnancy & Breastfeeding Scot-Tussin Expectorant SF Cough Support Group 0 Reviews for Scot-Tussin Expectorant SF Cough - Add your own review/rating Compare Scot-Tussin Expectorant SF Cough with other medications Bronchitis Cough


Download




Sucrets 4-Hour Cough Drops Lozenges


Pronunciation: DEX-troe-meth-OR-fan
Generic Name: Dextromethorphan
Brand Name: Examples include Hold and Sucrets 4-Hour Cough Drops
Sucrets 4-Hour Cough Drops Lozenges are used for:

Temporarily relieving cough due to the common cold, upper respiratory tract infections, sinus inflammation, sore throat, or bronchitis.

Sucrets 4-Hour Cough Drops Lozenges are a cough suppressant. It works by loosening mucus and lung secretions in the chest and making coughs more productive.

Do NOT use Sucrets 4-Hour Cough Drops Lozenges if: you are allergic to any ingredient in Sucrets 4-Hour Cough Drops Lozenges you are taking or have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using Sucrets 4-Hour Cough Drops Lozenges:

Some medical conditions may interact with Sucrets 4-Hour Cough Drops Lozenges. Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, plan to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have chronic cough, chronic bronchitis or any breathing problems, such as asthma, emphysema, chronic obstructive pulmonary disease (COPD), or if cough occurs with a large amount of mucus

Some MEDICINES MAY INTERACT with Sucrets 4-Hour Cough Drops Lozenges. Tell your health care provider if you are taking any other medicines, especially any of the following:

Furazolidone or MAO inhibitors (eg, phenelzine ) because the risk of toxic side effects may be increased by Sucrets 4-Hour Cough Drops Lozenges

This may not be a complete list of all interactions that may occur. Ask your health care provider if Sucrets 4-Hour Cough Drops Lozenges may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Sucrets 4-Hour Cough Drops Lozenges:

Use Sucrets 4-Hour Cough Drops Lozenges as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Sucrets 4-Hour Cough Drops Lozenges may be taken with or without food. Take with food if stomach upset occurs. Dissolve the medicine slowly in the mouth. Do not swallow whole. If you miss a dose of Sucrets 4-Hour Cough Drops Lozenges and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Sucrets 4-Hour Cough Drops Lozenges.

Important safety information: Sucrets 4-Hour Cough Drops Lozenges may cause drowsiness, dizziness, blurred vision, or lightheadedness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Sucrets 4-Hour Cough Drops Lozenges. Using Sucrets 4-Hour Cough Drops Lozenges alone, with certain other medicines, or with alcohol may lessen your ability to drive or to perform other potentially dangerous tasks. If your cough lasts for more than 1 week or comes back, or if you also have a fever, rash, or persistent headache, contact your health care provider. A persistent cough could be a sign of a serious condition. Sucrets 4-Hour Cough Drops Lozenges contains dextromethorphan. Before you being taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains dextromethorphan. If it does or if you are not sure, contact your health care provider or pharmacist. Phenylketonuria patients - Sucrets 4-Hour Cough Drops Lozenges contains phenylalanine. Sucrets 4-Hour Cough Drops Lozenges are not recommended for use in CHILDREN younger than 2 years of age. Safety and effectiveness in this age group have not been confirmed. PREGNANCY and BREAST-FEEDING: If you are pregnant or plan on becoming pregnant, discuss with your doctor the benefits and risks of using Sucrets 4-Hour Cough Drops Lozenges during pregnancy. It is unknown if Sucrets 4-Hour Cough Drops Lozenges are excreted in breast milk. Do not breast-feed while taking Sucrets 4-Hour Cough Drops Lozenges. Possible side effects of Sucrets 4-Hour Cough Drops Lozenges:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; drowsiness; stomach upset.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Sucrets 4-Hour Cough side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include confusion; excitement; hallucinations; slowed breathing.

Proper storage of Sucrets 4-Hour Cough Drops Lozenges:

Store Sucrets 4-Hour Cough Drops Lozenges between 59 and 86 degrees F (15 and 30 degrees C), away from heat, moisture, and light. Do not store in the bathroom. Keep Sucrets 4-Hour Cough Drops Lozenges out of the reach of children and away from pets.

General information: If you have any questions about Sucrets 4-Hour Cough Drops Lozenges, please talk with your doctor, pharmacist, or other health care provider. Sucrets 4-Hour Cough Drops Lozenges are to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Sucrets 4-Hour Cough Drops Lozenges. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Sucrets 4-Hour Cough Drops resources Sucrets 4-Hour Cough Drops Side Effects (in more detail) Sucrets 4-Hour Cough Drops Use in Pregnancy & Breastfeeding Sucrets 4-Hour Cough Drops Drug Interactions Sucrets 4-Hour Cough Drops Support Group 0 Reviews for Sucrets 4-Hour Cough - Add your own review/rating Compare Sucrets 4-Hour Cough Drops with other medications Cough


Download




PediaCare Long-Acting Cough Freezer Pops


Pronunciation: DEX-troe-meth-OR-fan
Generic Name: Dextromethorphan
Brand Name: PediaCare Long-Acting Cough
PediaCare Long-Acting Cough Freezer Pops are used for:

Temporarily relieving cough due to the common cold, hay fever, upper respiratory tract infections, sinus inflammation, sore throat, or bronchitis.

PediaCare Long-Acting Cough Freezer Pops are a cough suppressant. It works in the cough center of the brain to reduce a dry or nonproductive cough.

Do NOT use PediaCare Long-Acting Cough Freezer Pops if: you are allergic to any ingredient in PediaCare Long-Acting Cough Freezer Pops you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using PediaCare Long-Acting Cough Freezer Pops:

Some medical conditions may interact with PediaCare Long-Acting Cough Freezer Pops. Tell your health care provider if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have a history of chronic cough, asthma, lung problems (eg, chronic bronchitis, emphysema), chronic obstructive pulmonary disease (COPD), or if cough occurs with a large amount of mucus

Some MEDICINES MAY INTERACT with PediaCare Long-Acting Cough Freezer Pops. Tell your health care provider if you are taking any other medicines, especially any of the following:

Furazolidone or MAO inhibitors (eg, phenelzine) because the risk of serious side effects, such as severe low blood pressure, fever, severe muscle problems, and possibly death, may be increased by PediaCare Long-Acting Cough Freezer Pops

This may not be a complete list of all interactions that may occur. Ask your health care provider if PediaCare Long-Acting Cough Freezer Pops may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use PediaCare Long-Acting Cough Freezer Pops:

Use PediaCare Long-Acting Cough Freezer Pops as directed by your doctor. Check the label on the medicine for exact dosing instructions.

PediaCare Long-Acting Cough Freezer Pops may be taken with or without food. If stomach upset occurs, take with food to reduce stomach irritation. To use, cut off the top of the freezer pop sleeve and push freezer pop up from the bottom. PediaCare Long-Acting Cough Freezer Pops may be eaten frozen or the contents of 1 unfrozen sleeve may be poured into a cup or glass to drink. Immediately throw away any unused portion of the opened medicine. If you miss a dose of PediaCare Long-Acting Cough Freezer Pops and you are taking it regularly, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use PediaCare Long-Acting Cough Freezer Pops.

Important safety information: PediaCare Long-Acting Cough Freezer Pops may cause drowsiness, dizziness, blurred vision, or lightheadedness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to PediaCare Long-Acting Cough Freezer Pops. Using PediaCare Long-Acting Cough Freezer Pops alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks. If your cough lasts for more than 1 week or comes back, or if you also have a fever, rash, or persistent headache, contact your doctor. A persistent cough could be a sign of a serious condition. PediaCare Long-Acting Cough Freezer Pops contains dextromethorphan. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains dextromethorphan. If it does or if you are not sure, contact your doctor or pharmacist. Diabetes patients - Some brands of PediaCare Long-Acting Cough Freezer Pops may contain sugar and affect your blood sugar level. Read the label carefully before using PediaCare Long-Acting Cough Freezer Pops. PediaCare Long-Acting Cough Freezer Pops are not recommended for use in CHILDREN younger than 2 years of age. Safety and effectiveness in this age group have not been confirmed. PREGNANCY and BREAST-FEEDING: It is unknown if PediaCare Long-Acting Cough Freezer Pops can cause harm to the fetus. If you become pregnant while taking PediaCare Long-Acting Cough Freezer Pops, discuss with your doctor the benefits and risks of using PediaCare Long-Acting Cough Freezer Pops during pregnancy. It is unknown if PediaCare Long-Acting Cough Freezer Pops are excreted in breast milk. Do not breast-feed while taking PediaCare Long-Acting Cough Freezer Pops. Possible side effects of PediaCare Long-Acting Cough Freezer Pops:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; drowsiness; stomach upset.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: PediaCare Long-Acting Cough side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include confusion; excitement; hallucinations; slowed breathing.

Proper storage of PediaCare Long-Acting Cough Freezer Pops:

Store PediaCare Long-Acting Cough Freezer Pops at 77 degrees F (25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep PediaCare Long-Acting Cough Freezer Pops out of the reach of children and away from pets.

General information: If you have any questions about PediaCare Long-Acting Cough Freezer Pops, please talk with your doctor, pharmacist, or other health care provider. PediaCare Long-Acting Cough Freezer Pops are to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about PediaCare Long-Acting Cough Freezer Pops. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More PediaCare Long-Acting Cough resources PediaCare Long-Acting Cough Side Effects (in more detail) PediaCare Long-Acting Cough Use in Pregnancy & Breastfeeding PediaCare Long-Acting Cough Drug Interactions 0 Reviews for PediaCare Long-Acting Cough - Add your own review/rating Compare PediaCare Long-Acting Cough with other medications Cough


Download




Little Colds Decongestant/Cough Drops


Pronunciation: DEX-troe-meth-OR-fan/FEN-il-EF-rin
Generic Name: Dextromethorphan/Phenylephrine
Brand Name: Examples include Albatussin Pediatric Drops and Little Colds Decongestant/Cough
Little Colds Decongestant/Cough Drops are used for:

Relieving congestion and cough due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.

Little Colds Decongestant/Cough Drops are a decongestant and cough suppressant combination. It works by constricting blood vessels and reducing swelling in the nasal passages, which helps you to breathe more easily. The cough suppressant works in the brain to help decrease the cough reflex.

Do NOT use Little Colds Decongestant/Cough Drops if: you are allergic to any ingredient in Little Colds Decongestant/Cough Drops you have severe high blood pressure, rapid heartbeat, or other severe heart problems (eg, heart blood vessel disease) you have taken furazolidone or a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using Little Colds Decongestant/Cough Drops:

Some medical conditions may interact with Little Colds Decongestant/Cough Drops. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have a history of glaucoma, an enlarged prostate gland or other prostate problems, heart problems, diabetes, high blood pressure, blood vessel problems, adrenal gland problems, an overactive thyroid, seizures, or stroke if you have a history of chronic cough, chronic obstructive pulmonary disease (COPD), or other lung problems (eg, asthma, chronic bronchitis, emphysema), or if your cough produces large amounts of mucus

Some MEDICINES MAY INTERACT with Little Colds Decongestant/Cough Drops. Tell your health care provider if you are taking any other medicines, especially any of the following:

Beta-blockers (eg, propranolol), catechol-O-methyltransferase (COMT) inhibitors (eg, tolcapone), furazolidone, indomethacin, MAOIs (eg, phenelzine), or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Little Colds Decongestant/Cough Drops's side effects Digoxin or droxidopa because the risk of irregular heartbeat or heart attack may be increased Bromocriptine because the risk of its side effects may be increased by Little Colds Decongestant/Cough Drops Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because their effectiveness may be decreased by Little Colds Decongestant/Cough Drops

This may not be a complete list of all interactions that may occur. Ask your health care provider if Little Colds Decongestant/Cough Drops may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Little Colds Decongestant/Cough Drops:

Use Little Colds Decongestant/Cough Drops as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Little Colds Decongestant/Cough Drops by mouth with or without food. Use the dropper that comes with Little Colds Decongestant/Cough Drops to measure your dose. Ask your pharmacist for help if you are unsure of how to measure your dose. If you miss a dose of Little Colds Decongestant/Cough Drops, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Little Colds Decongestant/Cough Drops.

Important safety information: Little Colds Decongestant/Cough Drops may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Little Colds Decongestant/Cough Drops with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Do not take appetite suppressants while you are taking Little Colds Decongestant/Cough Drops without checking with your doctor. Little Colds Decongestant/Cough Drops has dextromethorphan and phenylephrine in it. Before you start any new medicine, check the label to see if it has dextromethorphan or phenylephrine in it too. If it does or if you are not sure, check with your doctor or pharmacist. Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor. If your symptoms do not get better within 5 to 7 days or if they get worse, check with your doctor. Little Colds Decongestant/Cough Drops may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Little Colds Decongestant/Cough Drops. Tell your doctor or dentist that you take Little Colds Decongestant/Cough Drops before you receive any medical or dental care, emergency care, or surgery. Use Little Colds Decongestant/Cough Drops with caution in the ELDERLY; they may be more sensitive to its effects. Caution is advised when using Little Colds Decongestant/Cough Drops in CHILDREN; they may be more sensitive to its effects. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Little Colds Decongestant/Cough Drops while you are pregnant. It is not known if Little Colds Decongestant/Cough Drops are found in breast milk. If you are or will be breast-feeding while you use Little Colds Decongestant/Cough Drops, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Little Colds Decongestant/Cough Drops:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; excitability; headache; nausea; nervousness or anxiety; trouble sleeping; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; tremor.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Little Colds Decongestant/Cough side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; vomiting.

Proper storage of Little Colds Decongestant/Cough Drops:

Store Little Colds Decongestant/Cough Drops at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Little Colds Decongestant/Cough Drops out of the reach of children and away from pets.

General information: If you have any questions about Little Colds Decongestant/Cough Drops, please talk with your doctor, pharmacist, or other health care provider. Little Colds Decongestant/Cough Drops are to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Little Colds Decongestant/Cough Drops. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Little Colds Decongestant/Cough resources Little Colds Decongestant/Cough Side Effects (in more detail)Little Colds Decongestant/Cough Use in Pregnancy & BreastfeedingLittle Colds Decongestant/Cough Drug Interactions0 Reviews for Little Colds Decongestant/Cough - Add your own review/rating Compare Little Colds Decongestant/Cough with other medications Cough and Nasal Congestion


Download




Tylenol Infants Plus Cold/Cough Drops


Pronunciation: a-seet-a-MIN-oh-fen/dex-troe-meth-OR-fan/sue-doe-eh-FED-rin
Generic Name: Acetaminophen/Dextromethorphan/Pseudoephedrine
Brand Name: Tylenol Infants Plus Cold/Cough
Tylenol Infants Plus Cold/Cough Drops are used for:

Relieving pain, congestion, and cough due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.

Tylenol Infants Plus Cold/Cough Drops are an analgesic, decongestant, and cough suppressant combination. It works by constricting blood vessels and reducing swelling in the nasal passages, which helps you breathe more easily. The analgesic and cough suppressant work in the brain to decrease pain and reduce the cough reflex.

Do NOT use Tylenol Infants Plus Cold/Cough Drops if: you are allergic to any ingredient in Tylenol Infants Plus Cold/Cough Drops you have severe high blood pressure, rapid heartbeat, or other severe heart problems (eg, heart blood vessel disease) you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using Tylenol Infants Plus Cold/Cough Drops:

Some medical conditions may interact with Tylenol Infants Plus Cold/Cough Drops. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have a history of glaucoma, an enlarged prostate gland or other prostate problems, heart problems, diabetes, high blood pressure, blood vessel problems, adrenal gland problems, an overactive thyroid, seizures, stroke, or liver problems, or if you consume more than 3 alcohol-containing drinks per day if you have a history of asthma, chronic cough, chronic obstructive pulmonary disease (COPD), or other lung problems (eg, chronic bronchitis, emphysema), or if your cough produces large amounts of mucus

Some MEDICINES MAY INTERACT with Tylenol Infants Plus Cold/Cough Drops. Tell your health care provider if you are taking any other medicines, especially any of the following:

Beta-blockers (eg, propranolol), COMT inhibitors (eg, tolcapone), furazolidone, indomethacin, isoniazid, MAO inhibitors (eg, phenelzine), or tricyclic antidepressants (eg, amitriptyline) because the risk of side effects from Tylenol Infants Plus Cold/Cough Drops may be increased Anticoagulants (eg, warfarin), digoxin, or droxidopa because the risk of side effects such as bleeding, irregular heartbeat, or heart attack may be increased Bromocriptine because the risk of side effects may be increased by Tylenol Infants Plus Cold/Cough Drops Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because their effectiveness may be decreased by Tylenol Infants Plus Cold/Cough Drops

This may not be a complete list of all interactions that may occur. Ask your health care provider if Tylenol Infants Plus Cold/Cough Drops may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Tylenol Infants Plus Cold/Cough Drops:

Use Tylenol Infants Plus Cold/Cough Drops as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Tylenol Infants Plus Cold/Cough Drops may be taken with or without food. Use the dropper that comes with Tylenol Infants Plus Cold/Cough Drops to measure your dose. Ask your pharmacist for help if you are unsure of how to measure your dose. If you miss a dose of Tylenol Infants Plus Cold/Cough Drops, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Tylenol Infants Plus Cold/Cough Drops.

Important safety information: Tylenol Infants Plus Cold/Cough Drops may cause dizziness or drowsiness. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Tylenol Infants Plus Cold/Cough Drops. Using Tylenol Infants Plus Cold/Cough Drops alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks. Do not take appetite suppressants while you are taking Tylenol Infants Plus Cold/Cough Drops without checking with your doctor. Tylenol Infants Plus Cold/Cough Drops contains acetaminophen and pseudoephedrine. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains acetaminophen or pseudoephedrine. If it does or if you are uncertain, contact your doctor or pharmacist. Do NOT exceed the recommended dose or take Tylenol Infants Plus Cold/Cough Drops for longer than prescribed without checking with your doctor. If your symptoms do not improve within 5 to 7 days or if they become worse, check with your doctor. Tylenol Infants Plus Cold/Cough Drops may cause liver damage. If you consume 3 or more alcohol-containing drinks every day, ask your doctor if you should take Tylenol Infants Plus Cold/Cough Drops or other pain relievers/fever reducers. Alcohol use combined with Tylenol Infants Plus Cold/Cough Drops may increase your risk for liver damage. Tylenol Infants Plus Cold/Cough Drops may interfere with certain lab test results. Make sure that all of your doctors and lab personnel know that you are taking Tylenol Infants Plus Cold/Cough Drops. Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Tylenol Infants Plus Cold/Cough Drops. Use Tylenol Infants Plus Cold/Cough Drops with caution in the ELDERLY because they may be more sensitive to its effects. Caution is advised when using Tylenol Infants Plus Cold/Cough Drops in CHILDREN because they may be more sensitive to its effects. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Tylenol Infants Plus Cold/Cough Drops, discuss with your doctor the benefits and risks of using Tylenol Infants Plus Cold/Cough Drops during pregnancy. It is unknown if Tylenol Infants Plus Cold/Cough Drops are excreted in breast milk. Do not breast-feed while taking Tylenol Infants Plus Cold/Cough Drops. Possible side effects of Tylenol Infants Plus Cold/Cough Drops:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; excitability; headache; nausea; nervousness or anxiety; trouble sleeping; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; stomach pain; tremor; yellowing of skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Tylenol Infants Plus Cold/Cough side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; stomach pain; unusually fast, slow, or irregular heartbeat; vomiting; yellowing of skin or eyes.

Proper storage of Tylenol Infants Plus Cold/Cough Drops:

Store Tylenol Infants Plus Cold/Cough Drops at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Tylenol Infants Plus Cold/Cough Drops out of the reach of children and away from pets.

General information: If you have any questions about Tylenol Infants Plus Cold/Cough Drops, please talk with your doctor, pharmacist, or other health care provider. Tylenol Infants Plus Cold/Cough Drops are to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Tylenol Infants Plus Cold/Cough Drops. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Tylenol Infants Plus Cold/Cough resources Tylenol Infants Plus Cold/Cough Side Effects (in more detail) Tylenol Infants Plus Cold/Cough Use in Pregnancy & Breastfeeding Tylenol Infants Plus Cold/Cough Drug Interactions Tylenol Infants Plus Cold/Cough Support Group 1 Review for Tylenol Infants Plus Cold/Cough - Add your own review/rating Compare Tylenol Infants Plus Cold/Cough with other medications Cold Symptoms


Download




Comtrex Cold and Cough Maximum Strength


Pronunciation: a-SEET-a-MIN-oh-fen/DEX-troe-meth-OR-fan/FEN-il-EF-rin
Generic Name: Acetaminophen/Dextromethorphan/Phenylephrine
Brand Name: Examples include Comtrex Cold and Cough Maximum Strength and Vicks DayQuil Multi-Symptom Cold/Flu Relief
Comtrex Cold and Cough Maximum Strength is used for:

Relieving pain, congestion, and cough due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.

Comtrex Cold and Cough Maximum Strength is an analgesic, cough suppressant, and decongestant combination. The analgesic and cough suppressant work in the brain to decrease pain and reduce the cough reflex. The decongestant works by constricting blood vessels and reducing swelling in the nasal passages, which helps you breathe more easily.

Do NOT use Comtrex Cold and Cough Maximum Strength if: you are allergic to any ingredient in Comtrex Cold and Cough Maximum Strength you have severe high blood pressure, rapid heartbeat, or other severe heart problems (eg, heart blood vessel disease) you have taken furazolidone or a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using Comtrex Cold and Cough Maximum Strength:

Some medical conditions may interact with Comtrex Cold and Cough Maximum Strength. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have a history of glaucoma, an enlarged prostate gland or other prostate problems, heart problems, diabetes, high blood pressure, blood vessel problems, adrenal gland problems, an overactive thyroid, seizures, stroke, liver problems (eg, hepatitis), or severe kidney problems, or if you drink more than 3 alcohol-containing drinks per day if you have a history of asthma, chronic cough, chronic obstructive pulmonary disease (COPD), or other lung problems (eg, chronic bronchitis, emphysema), or if your cough produces large amounts of mucus

Some MEDICINES MAY INTERACT with Comtrex Cold and Cough Maximum Strength. Tell your health care provider if you are taking any other medicines, especially any of the following:

Beta-blockers (eg, propranolol), catechol-O-methyltransferase (COMT) inhibitors (eg, tolcapone), furazolidone, indomethacin, isoniazid, MAOIs (eg, phenelzine), or tricyclic antidepressants (eg, amitriptyline) because they may increase the risk of Comtrex Cold and Cough Maximum Strength's side effects. Anticoagulants (eg, warfarin), digoxin, or droxidopa because the risk of side effects, such as bleeding, irregular heartbeat, or heart attack, may be increased Bromocriptine because the risk of its side effects may be increased by Comtrex Cold and Cough Maximum Strength Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because their effectiveness may be decreased by Comtrex Cold and Cough Maximum Strength

This may not be a complete list of all interactions that may occur. Ask your health care provider if Comtrex Cold and Cough Maximum Strength may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Comtrex Cold and Cough Maximum Strength:

Use Comtrex Cold and Cough Maximum Strength as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Take Comtrex Cold and Cough Maximum Strength by mouth with or without food. If you miss a dose of Comtrex Cold and Cough Maximum Strength, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Comtrex Cold and Cough Maximum Strength.

Important safety information: Comtrex Cold and Cough Maximum Strength may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Comtrex Cold and Cough Maximum Strength with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Do not take diet or appetite control medicines while you are taking Comtrex Cold and Cough Maximum Strength without checking with your doctor. Comtrex Cold and Cough Maximum Strength has acetaminophen, dextromethorphan, and phenylephrine in it. Before you start any new medicine, check the label to see if it has acetaminophen, dextromethorphan, or phenylephrine in it too. If it does or if you are not sure, check with your doctor or pharmacist. Do not use Comtrex Cold and Cough Maximum Strength for a cough with a lot of mucous. Do not use it for a long-term cough (eg, caused by asthma, emphysema, smoking). However, you may use it for these conditions if your doctor tells you to. Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor. If your symptoms do not get better within 5 to 7 days or if they become worse, check with your doctor. Comtrex Cold and Cough Maximum Strength may harm your liver. Your risk may be greater if you drink alcohol while you are using Comtrex Cold and Cough Maximum Strength. Talk to your doctor before you take Comtrex Cold and Cough Maximum Strength or other fever reducers if you drink more than 3 drinks with alcohol per day. Comtrex Cold and Cough Maximum Strength may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Comtrex Cold and Cough Maximum Strength. Tell your doctor or dentist that you take Comtrex Cold and Cough Maximum Strength before you receive any medical or dental care, emergency care, or surgery. Use Comtrex Cold and Cough Maximum Strength with caution in the ELDERLY; they may be more sensitive to its effects. Comtrex Cold and Cough Maximum Strength should be used with extreme caution in CHILDREN; they may be more sensitive to its effects. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Comtrex Cold and Cough Maximum Strength while you are pregnant. It is not known if Comtrex Cold and Cough Maximum Strength is found in breast milk. Do not breast-feed while taking Comtrex Cold and Cough Maximum Strength. Possible side effects of Comtrex Cold and Cough Maximum Strength:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; excitability; headache; nausea; nervousness or anxiety; trouble sleeping; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; stomach pain; tremor; yellowing of skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Comtrex Cold and Cough Maximum Strength side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; stomach pain; unusually fast, slow, or irregular heartbeat; vomiting; yellowing of skin or eyes.

Proper storage of Comtrex Cold and Cough Maximum Strength:

Store Comtrex Cold and Cough Maximum Strength between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Comtrex Cold and Cough Maximum Strength out of the reach of children and away from pets.

General information: If you have any questions about Comtrex Cold and Cough Maximum Strength, please talk with your doctor, pharmacist, or other health care provider. Comtrex Cold and Cough Maximum Strength is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Comtrex Cold and Cough Maximum Strength. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Comtrex Cold and Cough Maximum Strength resources Comtrex Cold and Cough Maximum Strength Side Effects (in more detail) Comtrex Cold and Cough Maximum Strength Use in Pregnancy & Breastfeeding Comtrex Cold and Cough Maximum Strength Drug Interactions 0 Reviews for Comtrex Cold and Cough Maximum Strength - Add your own review/rating Compare Comtrex Cold and Cough Maximum Strength with other medications Cold Symptoms Cough Cough and Nasal Congestion Nasal Congestion Pain/Fever Sinus Symptoms Tonsillitis/Pharyngitis


Download




Tylenol Cough/Sore Throat Liquid


Pronunciation: a-seet-a-MIN-oh-fen/dex-troe-meth-OR-fan/dox-IL-a-meen
Generic Name: Acetaminophen/Dextromethorphan/Doxylamine
Brand Name: Clear Cough PM Multi-Symptom and Tylenol Cough/Sore Throat
Tylenol Cough/Sore Throat Liquid is used for:

Relieving symptoms of pain, sinus congestion, runny nose, sneezing, and cough due to colds, upper respiratory infections, and allergies. It may also be used for other conditions as determined by your doctor.

Tylenol Cough/Sore Throat Liquid is an analgesic, cough suppressant, and antihistamine combination. The analgesic and cough suppressant work in the brain to decrease pain and to reduce dry or unproductive cough. The antihistamine works by blocking the action of histamine, which helps reduce symptoms, such as watery eyes and sneezing.

Do NOT use Tylenol Cough/Sore Throat Liquid if: you are allergic to any ingredient in Tylenol Cough/Sore Throat Liquid you are unable to urinate or are having an asthma attack you take sodium oxybate (GHB) or you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

Contact your doctor or health care provider right away if any of these apply to you.

Before using Tylenol Cough/Sore Throat Liquid:

Some medical conditions may interact with Tylenol Cough/Sore Throat Liquid. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement if you have allergies to medicines, foods, or other substances if you have a fast, slow, or irregular heartbeat if you have a history of heart problems; high blood pressure; diabetes; heart blood vessel problems; stroke; glaucoma; a blockage of your bladder, stomach, or intestines; ulcers; trouble urinating; an enlarged prostate or other prostate problems; seizures; an overactive thyroid; liver problems; severe kidney problems; or if you consume more than 3 alcohol-containing drinks per day if you have a history of asthma, chronic cough, lung problems (eg, chronic bronchitis, emphysema), or chronic obstructive pulmonary disease (COPD), or if cough occurs with large amounts of mucus

Some MEDICINES MAY INTERACT with Tylenol Cough/Sore Throat Liquid. Tell your health care provider if you are taking any other medicines, especially any of the following:

Beta-blockers (eg, propranolol), furazolidone, isoniazid, MAO inhibitors (eg, phenelzine), sodium oxybate (GHB), or tricyclic antidepressants (eg, amitriptyline) because side effects of Tylenol Cough/Sore Throat Liquid may be increased Anticoagulants (eg, warfarin) because risk of bleeding, irregular heartbeat or heart attack may be increased Hydantoins (eg, phenytoin) because side effects may be increased by Tylenol Cough/Sore Throat Liquid

This may not be a complete list of all interactions that may occur. Ask your health care provider if Tylenol Cough/Sore Throat Liquid may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

How to use Tylenol Cough/Sore Throat Liquid:

Use Tylenol Cough/Sore Throat Liquid as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Tylenol Cough/Sore Throat Liquid may be taken with or without food. Use a measuring device marked for medicine dosing. Ask your pharmacist for help if you are unsure of how to measure your dose. If you miss a dose of Tylenol Cough/Sore Throat Liquid, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Tylenol Cough/Sore Throat Liquid.

Important safety information: Tylenol Cough/Sore Throat Liquid may cause dizziness, drowsiness, or blurred vision. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Tylenol Cough/Sore Throat Liquid. Using Tylenol Cough/Sore Throat Liquid alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks. Do not take diet or appetite control medicines while you are taking Tylenol Cough/Sore Throat Liquid without checking with your doctor. Tylenol Cough/Sore Throat Liquid contains acetaminophen, doxylamine, and dextromethorphan. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains acetaminophen, doxylamine, or dextromethorphan. If it does or if you are uncertain, contact your doctor or pharmacist. Do NOT exceed the recommended dose or take Tylenol Cough/Sore Throat Liquid for longer than prescribed without checking with your doctor. If your symptoms do not improve within 5 to 7 days or if they become worse, check with your doctor. Tylenol Cough/Sore Throat Liquid may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to Tylenol Cough/Sore Throat Liquid. Use a sunscreen or protective clothing if you must be outside for a prolonged period. Tylenol Cough/Sore Throat Liquid may cause liver damage. If you consume 3 or more alcohol-containing drinks every day, ask your doctor if you should take Tylenol Cough/Sore Throat Liquid or other pain relievers/fever reducers. Alcohol use combined with Tylenol Cough/Sore Throat Liquid may increase your risk for liver damage. If you are scheduled for allergy skin testing, do not take Tylenol Cough/Sore Throat Liquid for several days before the test because it may decrease your response to the skin tests. Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Tylenol Cough/Sore Throat Liquid. Use Tylenol Cough/Sore Throat Liquid with caution in the ELDERLY because they may be more sensitive to its effects. Caution is advised when using Tylenol Cough/Sore Throat Liquid in CHILDREN because they may be more sensitive to its effects. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Tylenol Cough/Sore Throat Liquid, discuss with your doctor the benefits and risks of using Tylenol Cough/Sore Throat Liquid during pregnancy. It is unknown if Tylenol Cough/Sore Throat Liquid is excreted in breast milk. Do not breast-feed while taking Tylenol Cough/Sore Throat Liquid. Possible side effects of Tylenol Cough/Sore Throat Liquid:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Constipation; diarrhea; dizziness; drowsiness; excitability; headache; loss of appetite; nausea; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating or inability to urinate; fast or irregular heartbeat; hallucinations; seizures; severe dizziness, lightheadedness, or headache; stomach pain; tremor; trouble sleeping; vision changes; yellowing of skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

See also: Tylenol Cough/Sore Throat side effects (in more detail)

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include blurred vision; confusion; hallucinations; seizures; severe dizziness, lightheadedness, or headache; severe drowsiness; unusually fast, slow, or irregular heartbeat; and vomiting.

Proper storage of Tylenol Cough/Sore Throat Liquid:

Store Tylenol Cough/Sore Throat Liquid at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Tylenol Cough/Sore Throat Liquid out of the reach of children and away from pets.

General information: If you have any questions about Tylenol Cough/Sore Throat Liquid, please talk with your doctor, pharmacist, or other health care provider. Tylenol Cough/Sore Throat Liquid is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor. Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Tylenol Cough/Sore Throat Liquid. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.

Issue Date: February 1, 2012 Database Edition 12.1.1.002 Copyright © 2012 Wolters Kluwer Health, Inc. More Tylenol Cough/Sore Throat resources Tylenol Cough/Sore Throat Side Effects (in more detail) Tylenol Cough/Sore Throat Use in Pregnancy & Breastfeeding Tylenol Cough/Sore Throat Drug Interactions 0 Reviews for Tylenol Cough/Sore Throat - Add your own review/rating Compare Tylenol Cough/Sore Throat with other medications Cough Pain


Download




Tylenol Cough/Sore Throat Liquid


Related Posts Covonia Chesty Cough Mixture Mentholated:



Search


 

Best ED Pills

 

Erectile Dysfunction

 

RX Pharmacy Drugs List - Buy Pills Online

RSS | Site Map | Map | PageMap

Copyright © Online Pharmacy Drug Store. All rights reserved.