what does DMY012003 04/2014 mean on a blister pack of tablets
 

Pills
 

ED Pills

ED Drugs
 

Sentry HC Worm X



Dosage Form: FOR ANIMAL USE ONLY
Broad Spectrum De-Wormer Chewable Tablets for Large Dogs INDICATIONS & USAGE

For Removal of Hookworms in Puppies and Dogs

Ancylostoma caninum Uncinaria stenocephala For Removal of Large Roundworms (Ascarids) in Puppies and Dogs
Toxocara canis Toxascaris leonina To Prevent Reinfection of Large Roundworms in Puppies, Adult Dogs and Lactating Bitches After Whelping
Toxocara canis ACTIVE INGREDIENT (in each chewable) Pyrantel Pamoate (113.5 mg) How is Sentry HC Worm X Supplied Net Contents:    2 Tablet Count
Net Contents:    4 Tablet Count
Net Contents:  12 Tablet Count STORAGE Store at controlled room temperature of 59-86 degrees F (15-30 degrees C). PACKAGE LABEL PRINCIPAL DISPLAY PANEL Sentry HC Worm X
Distributed by:
Sergeant's Pet Care Products, Inc., Omaha NE 68130
www.sentrypetcare.com
ANADA #200-281, Approved by FDA
Sentry HC Worm X 
pyrantel pamoate  tablet, chewable Product Information Product Type OTC ANIMAL DRUG NDC Product Code (Source) 21091-402 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRANTEL PAMOATE (PYRANTEL) PYRANTEL PAMOATE 113.5 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color brown Score no score Shape ROUND Size 10mm Flavor LIVER (Pork Liver Powder) Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 21091-402-02 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 2 TABLET In 1 BLISTER PACK This package is contained within the CARTON (21091-402-02) 2 21091-402-04 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 4 TABLET In 1 BLISTER PACK This package is contained within the CARTON (21091-402-04) 3 21091-402-12 6 BLISTER PACK In 1 CARTON contains a BLISTER PACK 3 12 TABLET In 1 BLISTER PACK This package is contained within the CARTON (21091-402-12)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANADA ANADA200281 01/16/2008
Labeler - Sergeant's Pet Care Products, Inc. (876995171) Establishment Name Address ID/FEI Operations Virbac Bridgeton 808558100 manufacture Revised: 11/2010Sergeant's Pet Care Products, Inc.

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Allergy Relief Tablets


loratadine
Dosage Form: tablet
Drug Facts Active ingredient

loratadine 10mg

Purpose

antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

• runny nose • itchy, watery eyes • sneezing • itching of the nose or throat

Warnings Adverse Reactions Do Not Use

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask Doctor

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

When Using

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Stop Use

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

Pregnancy or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep Out of Reach of Children

Keep out of reach of children.

Overdose

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

Other Information safety sealed: do not use if the imprinted bottle seal with “sealed for your protection” is open or torn (for bottle carton only) safety sealed: do not use if the imprinted blister unit is open or torn (for blister carton only) store at 20-25°C (68-77°F) (see USP Controlled Room Temperature) Directions adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor Inactive ingredients

lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions

call 1-800-452-0051

 

 Distributed by Target Corp.

Minneapolis, MN 55403

copyright 2009 Target Brands, Inc.

All Rights Persevered

Principal Display

Target


ALLERGY RELIEF MEDICATION 
loratadine  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 11673-315 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (LORATADINE) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength CELLULOSE, MICROCRYSTALLINE   LACTOSE MONOHYDRATE   MAGNESIUM STEARATE   SODIUM STARCH GLYCOLATE TYPE A POTATO   Product Characteristics Color WHITE Score no score Shape ROUND Size 6mm Flavor Imprint Code GG;296 Contains          Packaging # NDC Package Description Multilevel Packaging 1 11673-315-10 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 5 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11673-315-10) 2 11673-315-40 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11673-315-40) 3 11673-315-18 1 BOTTLE In 1 CARTON contains a BOTTLE 3 180 TABLET In 1 BOTTLE This package is contained within the CARTON (11673-315-18) 4 11673-315-60 6 BLISTER PACK In 1 CARTON contains a BLISTER PACK 4 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11673-315-60) 5 11673-315-30 3 BLISTER PACK In 1 CARTON contains a BLISTER PACK 5 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11673-315-30) 6 11673-315-15 3 BLISTER PACK In 1 CARTON contains a BLISTER PACK 6 5 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11673-315-15)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA075209 01/31/2010
Labeler - Target Brands, Inc. (006961700) Revised: 09/2010Target Brands, Inc. More Allergy Relief Tablets resources Allergy Relief Tablets Side Effects (in more detail) Allergy Relief Tablets Dosage Allergy Relief Tablets Use in Pregnancy & Breastfeeding Allergy Relief Tablets Drug Interactions 0 Reviews for Allergy Reliefs - Add your own review/rating Compare Allergy Relief Tablets with other medications Hay Fever Urticaria
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Topcare Anti-Diarrheal


Generic Name: loperamide
Dosage Form: tablet
Topco Anti-Diarrheal Tablets Drug Facts Active ingredient (in each caplet)

Loperamide HCl 2 mg

Purpose

Anti-diarrheal

Uses

controls symptoms of diarrhea, including Travelers’ Diarrhea

Warnings

Allergy alert: Do not use if you have ever had a rash or other allergic reaction to loperamide HCl

Do not use

if you have bloody or black stool

Ask a doctor before use if you have fever mucus in the stool a history of liver disease Ask a doctor or pharmacist before use if you are

taking antibiotics

When using this product tiredness, drowsiness or dizziness may occur. Be careful when driving or operating machinery. Stop use and ask a doctor if symptoms get worse diarrhea lasts for more than 2 days you get abdominal swelling or bulging. These may be signs of a serious condition. If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions drink plenty of clear fluids to help prevent dehydration caused by diarrhea find right dose on chart. If possible, use weight to dose; otherwise, use age. adults and children 12 years and over 2 caplets after the first loose stool; 1 caplet after each subsequent loose stool; but no more than 4 caplets in 24 hours children 9-11 years (60-95 lbs) 1 caplet after the first loose stool; 1/2 caplet after each subsequent loose stool; but no more than 3 caplets in 24 hours children 6-8 years (48-59 lbs) 1 caplet after the first loose stool; 1/2 caplet after each subsequent loose stool; but no more than 2 caplets in 24 hours children under 6 years (up to 47 lbs) ask a doctor Other information store between 20-25°C (68-77°F) do not use if printed foil under cap is broken or missing (Bottle Only) do not use if carton or blister unit is broken or torn (Blister Only) see end panel for lot number and expiration date Inactive ingredients

anhydrous lactose, carnauba wax, D&C yellow no. 10, FD&C blue no. 1, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized starch

Questions or comments?

1-888-423-0139

Principal Display Panel

Easy to Swallow

Loperamide Hydrochloride Tablets, 2 mg

Anti-Diarrheal Tablets

Controls the Symptoms of Diarrhea, Including Travelers’ Diarrhea

Actual Size

Compare to Imodium® A-D active ingredient

Each Caplet (Capsule-Shaped Tablet) Contains 2 mg Loperamide Hydrochloride

Anti-Diarrheal Tablets Carton


TOPCARE ANTI DIARRHEAL 
loperamide hydrochloride  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 36800-224 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LOPERAMIDE HYDROCHLORIDE (LOPERAMIDE) LOPERAMIDE HYDROCHLORIDE 2 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color GREEN Score 2 pieces Shape CAPSULE Size 10mm Flavor Imprint Code L2 Contains          Packaging # NDC Package Description Multilevel Packaging 1 36800-224-91 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (36800-224-91) 2 36800-224-53 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (36800-224-53) 3 36800-224-62 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK 3 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (36800-224-62) 4 36800-224-80 1 BOTTLE In 1 CARTON contains a BOTTLE 4 96 TABLET In 1 BOTTLE This package is contained within the CARTON (36800-224-80)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA075232 02/26/2003
Labeler - Topco Associates LLC (006935977) Revised: 08/2009Topco Associates LLC
More Topcare Anti-Diarrheal resources Topcare Anti-Diarrheal Side Effects (in more detail) Topcare Anti-Diarrheal Use in Pregnancy & Breastfeeding Drug Images Topcare Anti-Diarrheal Drug Interactions Topcare Anti-Diarrheal Support Group 8 Reviews for Topcare Anti-Diarrheal - Add your own review/rating Compare Topcare Anti-Diarrheal with other medications Diarrhea Diarrhea, Acute Diarrhea, Chronic Lymphocytic Colitis Traveler's Diarrhea
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Equaline Allergy Relief


loratadine
Dosage Form: tablet
SuperValu Allergy Relief Drug Facts Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

runny nose sneezing itchy, watery eyes itching of the nose or throat Warnings Do not use

if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product

do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other information do not use if blister unit is broken or torn (Blister Only) do not use if printed foil under cap is broken or missing (Bottle Only) store at 20°-25°C (68°-77°F) protect from excessive moisture (Blister Only) Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-877-932-7948

Principal Display Panel

Compare to Claritin® Tablets active ingredient

Non-Drowsy*

Allergy Relief

Loratadine Tablets, 10 mg/Antihistamine

Indoor & Outdoor Allergies

24 Hour Relief of:

Sneezing

Itchy, Watery Eyes

Runny Nose

Itchy Throat or Nose

Actual Size

Original Prescription Strength

*When taken as directed. See Drug Facts Panel.

Allergy Relief Carton


Equaline Allergy Relief 
loratadine  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 41163-612 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (LORATADINE) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE Score no score Shape OVAL Size 8mm Flavor Imprint Code L612 Contains          Packaging # NDC Package Description Multilevel Packaging 1 41163-612-46 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (41163-612-46) 2 41163-612-65 1 BOTTLE In 1 CARTON contains a BOTTLE 2 30 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-65) 3 41163-612-72 1 BOTTLE In 1 CARTON contains a BOTTLE 3 60 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-72) 4 41163-612-75 1 BOTTLE In 1 CARTON contains a BOTTLE 4 90 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-75) 5 41163-612-60 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 5 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (41163-612-60) 6 41163-612-95 1 BOTTLE In 1 CARTON contains a BOTTLE 6 45 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-95)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076301 02/07/2005
Labeler - Supervalu Inc (006961411) Revised: 09/2009Supervalu Inc
More Equaline Allergy Relief resources Equaline Allergy Relief Side Effects (in more detail) Equaline Allergy Relief Dosage Equaline Allergy Relief Use in Pregnancy & Breastfeeding Equaline Allergy Relief Drug Interactions 0 Reviews for Equaline Allergy Relief - Add your own review/rating Compare Equaline Allergy Relief with other medications Hay Fever Urticaria
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Good Sense Sleep Aid



Dosage Form: tablet
Perrigo Sleep Aid Tablets Drug Facts Active ingredient (in each tablet)

Doxylamine succinate 25 mg

Purpose

Nighttime sleep-aid

Uses helps to reduce difficulty in falling asleep Warnings

Ask a doctor before use if you have

a breathing problem such as asthma, emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland Do not give

to children under 12 years of age

Ask a doctor or pharmacist before use if you are

taking any other drugs

When using this product avoid alcoholic beverages take only at bedtime Stop use and ask a doctor if sleeplessness persists continuously for more than two weeks. Insomnia may be a symptom of serious underlying medical illness. If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 12 years of age and over: take one tablet 30 minutes before going to bed; take once daily or as directed by a doctor children under 12 years of age: do not use Other information store at 68°-77°F (20°-25°C) retain in carton until time of use see carton end panel for lot number and expiration date Inactive ingredients

dibasic calcium phosphate, FD&C blue no. 1 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

1-800-719-9260

Principal Display Panel

Fall Asleep Fast!

Sleep Aid Tablets

Doxylamine Succinate Tablets, 25 mg

Nighttime Sleep-Aid

Safe, Proven Effective

Just One Tablet Per Dose

Actual Size

Compare to active ingredient of Unisom® SleepTabs®

Sleep Aid Tablets Carton


Good Sense Sleep Aid 
doxylamine succinate  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0113-0441 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOXYLAMINE SUCCINATE (DOXYLAMINE) DOXYLAMINE SUCCINATE 25 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color BLUE Score no score Shape OVAL Size 10mm Flavor Imprint Code L441 Contains          Packaging # NDC Package Description Multilevel Packaging 1 0113-0441-64 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 16 TABLET In 1 BLISTER PACK This package is contained within the CARTON (0113-0441-64) 2 0113-0441-73 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 16 TABLET In 1 BLISTER PACK This package is contained within the CARTON (0113-0441-73)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA040167 04/14/1997
Labeler - L Perrigo Company (006013346) Revised: 06/2009L Perrigo Company
More Good Sense Sleep Aid resources Good Sense Sleep Aid Side Effects (in more detail)Good Sense Sleep Aid Use in Pregnancy & BreastfeedingDrug ImagesGood Sense Sleep Aid Drug InteractionsGood Sense Sleep Aid Support Group8 Reviews for Good Sense Sleep Aid - Add your own review/rating Compare Good Sense Sleep Aid with other medications AllergiesConjunctivitis, AllergicHay FeverInsomniaNasal CongestionRhinorrheaUpper Respiratory Tract Infection
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Mucinex DM


guaifenesin and dextromethorphan hydrobromide
Dosage Form: tablet, extended release
Mucinex®DM

600 mg guaifenesin & 30 mg dextromethorphan HBr extended-release bi-layer tablets

EXPECTORANT & COUGH SUPPRESSANT

Drug Facts

Active ingredients (in each extended-release bi-layer tablet) Purpose Dextromethorphan HBr 30 mg Cough suppressant Guaifenesin 600 mg Expectorant Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep Warnings

Do not use

for children under 12 years of age if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus)

When using this product

do not use more than directed

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions do not crush, chew, or break tablet take with a full glass of water this product can be administered without regard for timing of meals adults and children 12 years and older: 1 or 2 tablets every 12 hours; not more than 4 tablets in 24 hours children under 12 years of age: do not use Other information tamper evident: do not use if carton is open or if printed seal on blister is broken or missing store at 20-25°C (68-77°F) Inactive ingredients

carbomer 934P, NF; D&C yellow #10 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

Distributed by:
Reckitt Benckiser Inc.
Parsippany, NJ 07054-0224
©RBI 2009

PRINCIPAL DISPLAY PANEL - 600 mg Carton

NDC 63824-056-32

Mucinex®DM

600 mg guaifenesin & 30 mg dextromethorphan HBr
extended-release bi-layer tablets

EXPECTORANT & COUGH SUPPRESSANT

12 HOUR

NEW LOOK-
SAME RELIEF

Thins And Loosens Mucus

Controls Cough

20 EXTENDED-RELEASE BI-LAYER TABLETS


Mucinex DM 
guaifenesin and dextromethorphan hydrobromide  tablet, extended release Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 63824-056 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Guaifenesin (Guaifenesin) Guaifenesin 600 mg Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide 30 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE (yellow and white) Score no score Shape OVAL Size 16mm Flavor Imprint Code Mucinex;600 Contains          Packaging # NDC Package Description Multilevel Packaging 1 63824-056-32 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (63824-056-32) 2 63824-056-34 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (63824-056-34) 3 63824-056-58 1 BOTTLE In 1 CARTON contains a BOTTLE 3 58 TABLET In 1 BOTTLE This package is contained within the CARTON (63824-056-58) 4 63824-056-72 25 POUCH In 1 CARTON contains a POUCH 4 2 TABLET In 1 POUCH This package is contained within the CARTON (63824-056-72) 5 63824-056-76 3 POUCH In 1 CARTON contains a POUCH 5 2 TABLET In 1 POUCH This package is contained within the CARTON (63824-056-76)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021620 03/31/2009
Labeler - Reckitt Benckiser, Inc. (094405024) Revised: 12/2009Reckitt Benckiser, Inc.
More Mucinex DM resources Mucinex DM Side Effects (in more detail) Mucinex DM Dosage Mucinex DM Use in Pregnancy & Breastfeeding Mucinex DM Drug Interactions Mucinex DM Support Group 0 Reviews for Mucinex DM - Add your own review/rating Mucinex DM Concise Consumer Information (Cerner Multum) Anti-Tuss DM Concise Consumer Information (Cerner Multum) Atuss-12 DX Extended-Release Liquid MedFacts Consumer Leaflet (Wolters Kluwer) Bidex-A Extended-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer) Duratuss DM 12 Suspension MedFacts Consumer Leaflet (Wolters Kluwer) Guaifenesin DM Elixir MedFacts Consumer Leaflet (Wolters Kluwer) Humibid CS MedFacts Consumer Leaflet (Wolters Kluwer) Robitussin DM infant drops Scot-Tussin DM Liquid MedFacts Consumer Leaflet (Wolters Kluwer) Compare Mucinex DM with other medications Cough Expectoration
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Mucinex DM Maximum Strength


guaifenesin and dextromethorphan hydrobromide
Dosage Form: tablet, extended release
Mucinex®DM

Drug Facts

Active ingredients (in each extended-release bi-layer tablet) Purpose Dextromethorphan HBr 60 mg Cough suppressant Guaifenesin 1200 mg Expectorant Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep Warnings

Do not use

for children under 12 years of age if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus)

When using this product

do not use more than directed

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions do not crush, chew, or break tablet take with a full glass of water this product can be administered without regard for timing of meals adults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hours children under 12 years of age: do not use Other information tamper evident: do not use if carton is open or if printed seal on blister is broken or missing store at 20-25°C (68-77°F) Inactive ingredients

carbomer 934P, NF; D&C yellow #10 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

Distributed by:
Reckitt Benckiser Inc.
Parsippany, NJ 07054-0224
©RBI 2009

PRINCIPAL DISPLAY PANEL - 1200 mg Carton

MAXIMUM STRENGTH

NDC 63824-072-35

Mucinex®DM

1200 mg guaifenesin & 60 mg dextromethorphan HBr
extended-release bi-layer tablets

EXPECTORANT & COUGH SUPPRESSANT

12 HOUR

NEW LOOK-
SAME RELIEF

Thins And Loosens Mucus

Controls Cough

14 EXTENDED-RELEASE BI-LAYER TABLETS


MUCINEX DM  MAXIMUM STRENGTH
guaifenesin and dextromethorphan hydrobromide  tablet, extended release Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 63824-072 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Guaifenesin (Guaifenesin) Guaifenesin 1200 mg Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide 60 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE (yellow and white) Score no score Shape OVAL Size 22mm Flavor Imprint Code Mucinex;1200 Contains          Packaging # NDC Package Description Multilevel Packaging 1 63824-072-35 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 7 TABLET In 1 BLISTER PACK This package is contained within the CARTON (63824-072-35) 2 63824-072-36 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 7 TABLET In 1 BLISTER PACK This package is contained within the CARTON (63824-072-36) 3 63824-072-39 1 BOTTLE In 1 CARTON contains a BOTTLE 3 38 TABLET In 1 BOTTLE This package is contained within the CARTON (63824-072-39) 4 63824-072-45 1 BOTTLE In 1 CARTON contains a BOTTLE 4 44 TABLET In 1 BOTTLE This package is contained within the CARTON (63824-072-45)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021620 03/31/2009
Labeler - Reckitt Benckiser, Inc. (094405024) Revised: 12/2009Reckitt Benckiser, Inc.
More Mucinex DM Maximum Strength resources Mucinex DM Maximum Strength Side Effects (in more detail) Mucinex DM Maximum Strength Dosage Mucinex DM Maximum Strength Use in Pregnancy & Breastfeeding Mucinex DM Maximum Strength Drug Interactions Mucinex DM Maximum Strength Support Group 0 Reviews for Mucinex DM Maximum Strength - Add your own review/rating Allfen DM Concise Consumer Information (Cerner Multum) Anti-Tuss DM Concise Consumer Information (Cerner Multum) Atuss-12 DX Extended-Release Liquid MedFacts Consumer Leaflet (Wolters Kluwer) Bidex-A Extended-Release Tablets MedFacts Consumer Leaflet (Wolters Kluwer) Duratuss DM 12 Suspension MedFacts Consumer Leaflet (Wolters Kluwer) Guaifenesin DM Elixir MedFacts Consumer Leaflet (Wolters Kluwer) Humibid CS MedFacts Consumer Leaflet (Wolters Kluwer) Robitussin DM infant drops Scot-Tussin DM Liquid MedFacts Consumer Leaflet (Wolters Kluwer) Compare Mucinex DM Maximum Strength with other medications Cough Expectoration
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Loratadine Drug Facts


Dosage Form: tablet
Drug Facts Active Ingredient (in each tablet)

Loratadine, USP 10 mg

Purpose

Antihistamine

Uses

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

runny nose itchy, watery eyes sneezing itching of the nose or throat Warnings Do not use

if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have

liver or kidney disease.Your doctor should determine if you need a different dose.

When using this product

do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor

if an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other Information Safety sealed: do not use if the imprinted bottle seal is open or torn (for bottle only). Safety sealed: do not use if open or torn (for blister package only). Store at 20°-25°C (68°-77°F) (see USP Controlled Room Temperature). Inactive Ingredients

Lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate.

Questions or comments?

1-800-525-8747

05-2010M

Sandoz Inc.

Princeton, NJ 08540

mg Label

NDC 0781-5077-01 Non-Drowsy*

LORAtadine

Tablets, USP

10 mg

Antihistamine

Indoor & Outdoor Allergies

100 Tablets

SANDOZ

24 Hour

Relief of:

Sneezing

Runny Nose

Itchy, Watery

Eyes

Itchy Throat

or Nose

* When taken as directed.

See Drug Facts Panel.


mg Blister Pack

NDC 0781-5077-64

LORAtadine Tablets, USP 10 mg

10-2009M


mg Blister Pack Carton

NDC 0781-5077-64

Non-Drowsy*

LORAtadine

Tablets, USP

10 mg Antihistamine

Indoor & Outdoor Allergies

30 Tablets

SANDOZ

24 Hour

Relief of:

Sneezing

Runny Nose

Itchy, Watery

Eyes

Itchy Throat

or Nose


LORATADINE 
loratadine  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0781-5077 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (LORATADINE) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE   MAGNESIUM STEARATE   CELLULOSE, MICROCRYSTALLINE   SODIUM STARCH GLYCOLATE TYPE A POTATO   Product Characteristics Color WHITE (white to off white) Score no score Shape ROUND Size 6mm Flavor Imprint Code GG296 Contains          Packaging # NDC Package Description Multilevel Packaging 1 0781-5077-76 12 CARTON In 1 CARTON contains a CARTON (0781-5077-64) 1 0781-5077-64 1 BLISTER PACK In 1 CARTON This package is contained within the CARTON (0781-5077-76) and contains a BLISTER PACK 1 30 TABLET In 1 BLISTER PACK This package is contained within a CARTON (0781-5077-64) and a CARTON (0781-5077-76) 2 0781-5077-01 100 TABLET In 1 BOTTLE None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA075209 01/21/2003
Labeler - Sandoz Inc (110342024) Establishment Name Address ID/FEI Operations Sandoz Inc 110342024 MANUFACTURE Establishment Name Address ID/FEI Operations Thermo-Pak, Inc 161049044 PACK, LABEL Revised: 06/2010Sandoz Inc
More Loratadine Drug Facts resources Loratadine Drug Facts Side Effects (in more detail)Loratadine Drug Facts DosageLoratadine Drug Facts Use in Pregnancy & BreastfeedingDrug ImagesLoratadine Drug Facts Drug InteractionsLoratadine Drug Facts Support Group21 Reviews for Loratadine Drug Facts - Add your own review/rating Compare Loratadine Drug Facts with other medications Hay FeverUrticaria
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Healthy Accents Allergy Relief


loratadine
Dosage Form: tablets
DZA Brands, LLC Allergy Relief Drug Facts Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

runny nose sneezing itchy, watery eyes itching of the nose or throat Warnings Do not use

if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product

do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other information do not use if printed foil under cap is broken or missing (bottle only) do not use if blister unit is broken or torn (blister only) store at 20°-25°C (68°-77°F) Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-866-322-2439

Principal Display Panel

Compare to active ingredient of Claritin®

Allergy Relief

Loratadine Tablets, 10 mg/Antihistamine

24 Hour Relief of:

Sneezing

Runny Nose

Itchy, Watery Eyes

Itchy Throat or Nose

Non-Drowsy*

Indoor & Outdoor Allergies

Actual Size

*When taken as directed. See Drug Facts Panel.

Allergy Relief Carton


Healthy Accents Allergy Relief 
loratadine  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 55316-612 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (LORATADINE) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE Score no score Shape OVAL Size 8mm Flavor Imprint Code L612 Contains          Packaging # NDC Package Description Multilevel Packaging 1 55316-612-46 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (55316-612-46) 2 55316-612-65 1 BOTTLE In 1 CARTON contains a BOTTLE 2 30 TABLET In 1 BOTTLE This package is contained within the CARTON (55316-612-65) 3 55316-612-75 1 BOTTLE In 1 CARTON contains a BOTTLE 3 90 TABLET In 1 BOTTLE This package is contained within the CARTON (55316-612-75)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076301 12/15/2007
Labeler - DZA Brands LLC (090322194) Revised: 09/2009DZA Brands LLC
More Healthy Accents Allergy Relief resources Healthy Accents Allergy Relief Side Effects (in more detail) Healthy Accents Allergy Relief Dosage Healthy Accents Allergy Relief Use in Pregnancy & Breastfeeding Healthy Accents Allergy Relief Drug Interactions 0 Reviews for Healthy Accents Allergy Relief - Add your own review/rating Compare Healthy Accents Allergy Relief with other medications Hay Fever Urticaria
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Equaline Sleep Aid


doxylamine succinate
Dosage Form: tablet
SuperValu Sleep Aid Tablets Drug Facts Active ingredient (in each tablet)

Doxylamine succinate 25 mg

Purpose

Nighttime sleep-aid

Uses helps to reduce difficulty in falling asleep Warnings

Ask a doctor before use if you have

a breathing problem such as asthma, emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland Do not give

to children under 12 years of age

Ask a doctor or pharmacist before use if you are

taking any other drugs

When using this product avoid alcoholic beverages take only at bedtime Stop use and ask a doctor if sleeplessness persists continuously for more than two weeks. Insomnia may be a symptom of serious underlying medical illness. If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 12 years of age and over: take one tablet 30 minutes before going to bed; take once daily or as directed by a doctor children under 12 years of age: do not use Other information store at 68°-77°F (20°-25°C) retain in carton until time of use see carton end panel for lot number and expiration date Inactive ingredients

dibasic calcium phosphate, FD&C blue no. 1 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

1-877-932-7948

Principal Display Panel

Compare to Unisom® SleepTabs® active ingredient

Fall Asleep Fast

Safe

Sleep Aid

Tablets

Doxylamine Succinate Tablets, 25 mg

Nighttime Sleep-Aid

Proven Effective

Just One Tablet Per Dose

Actual Size

Sleep Aid Tablets Carton


Equaline Sleep Aid 
doxylamine succinate  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 41163-441 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOXYLAMINE SUCCINATE (DOXYLAMINE) DOXYLAMINE SUCCINATE 25 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color BLUE Score no score Shape OVAL Size 10mm Flavor Imprint Code L441 Contains          Packaging # NDC Package Description Multilevel Packaging 1 41163-441-67 3 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 16 TABLET In 1 BLISTER PACK This package is contained within the CARTON (41163-441-67)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA040167 08/10/2004
Labeler - Supervalu Inc (006961411) Revised: 06/2009Supervalu Inc
More Equaline Sleep Aid resources Equaline Sleep Aid DosageEqualine Sleep Aid Use in Pregnancy & BreastfeedingEqualine Sleep Aid Drug Interactions0 Reviews for Equaline Sleep Aid - Add your own review/rating Compare Equaline Sleep Aid with other medications AllergiesConjunctivitis, AllergicHay FeverInsomniaNasal CongestionRhinorrheaUpper Respiratory Tract Infection
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Mucinex D Maximum Strength



Dosage Form: tablet, extended release
Mucinex®D

Drug Facts

Active ingredients (in each extended-release bi-layer tablet) Purpose Guaifenesin 1200 mg Expectorant Pseudoephedrine HCl 120 mg Nasal Decongestant Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily relieves nasal congestion due to: common cold hay fever upper respiratory allergies temporarily restores freer breathing through the nose promotes nasal and/or sinus drainage temporarily relieves sinus congestion and pressure Warnings

Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

heart disease high blood pressure thyroid disease diabetes trouble urinating due to an enlarged prostate gland persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus)

When using this product

do not use more than directed

Stop use and ask a doctor if

you get nervous, dizzy, or sleepless symptoms do not get better within 7 days, come back or occur with a fever, rash, or persistent headache. These could be signs of a serious illness.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions do not crush, chew, or break tablet take with a full glass of water this product can be administered without regard for timing of meals adults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hours children under 12 years of age: do not use Other information tamper evident: do not use if carton is open or if printed seal on blister is broken or missing store at 20-25°C (68-77°F) Inactive ingredients

carbomer 934P, NF; FD&C yellow #6 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

Distributed by:
Reckitt Benckiser Inc.
Parsippany, NJ 07054-0224
©RBI 2009

PRINCIPAL DISPLAY PANEL - 1200 mg Carton

MAXIMUM STRENGTH

NDC 63824-041-24

Mucinex®D

1200 mg guaifenesin & 120 mg pseudoephedrine HCl
extended-release bi-layer tablets

EXPECTORANT & NASAL DECONGESTANT

12 HOUR

NEW LOOK-
SAME RELIEF

Thins And Loosens Mucus

Clears Nasal/Sinus Congestion

24 EXTENDED-RELEASE BI-LAYER TABLETS


MUCINEX D   MAXIMUM STRENGTH
guaifenesin and pseudoephedrine hydrochloride  tablet, extended release Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 63824-041 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Guaifenesin (Guaifenesin) Guaifenesin 1200 mg Pseudoephedrine Hydrochloride (Pseudoephedrine) Pseudoephedrine Hydrochloride 120 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color ORANGE, WHITE Score no score Shape OVAL Size 22mm Flavor Imprint Code Mucinex;1200 Contains          Packaging # NDC Package Description Multilevel Packaging 1 63824-041-24 3 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 8 TABLET In 1 BLISTER PACK This package is contained within the CARTON  (63824-041-24)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021585 04/17/2009
Labeler - Reckitt Benckiser, Inc. (094405024) Revised: 12/2009Reckitt Benckiser, Inc.
More Mucinex D Maximum Strength resources Mucinex D Maximum Strength Side Effects (in more detail) Mucinex D Maximum Strength Use in Pregnancy & Breastfeeding Drug Images Mucinex D Maximum Strength Drug Interactions Mucinex D Maximum Strength Support Group 58 Reviews for Mucinex D Maximum Strength - Add your own review/rating Compare Mucinex D Maximum Strength with other medications Cough and Nasal Congestion
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Wind-Eze Tablets


1. Name Of The Medicinal Product

Wind-Eze

2. Qualitative And Quantitative Composition

Simeticone [Equivalent to Poly(Dimethylsiloxane)], 11.57% w/w, approx. 125.00mg

3. Pharmaceutical Form

Chewable tablets for oral administration.

4. Clinical Particulars 4.1 Therapeutic Indications

Antiflatulent defoaming agent for the symptomatic relief of flatulence, wind pains, bloating, abdominal distension and other similar symptoms associated with gastrointestinal gas.

4.2 Posology And Method Of Administration

Adults, elderly and children over 12 years:

One tablet to be taken three or four times daily or as required for relief, after meals and upon retiring. The tablets are to be chewed before swallowing.

Not recommended for children under 12 years.

4.3 Contraindications

The product should not be used in patients with known hypersensitivity to any of the ingredients.

4.4 Special Warnings And Precautions For Use

If symptoms persist or worsen, medical advice should be sought.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

None known.

4.6 Pregnancy And Lactation

Since simeticone is not absorbed by the gastro intestinal tract, Wind-Eze may be taken during pregnancy and lactation.

4.7 Effects On Ability To Drive And Use Machines

None known.

4.8 Undesirable Effects

Rarely hypersensitivity reactions such as rash, pruritus, facial oedema, tongue oedema, respiratory difficulty.

4.9 Overdose

In the unlikely event of deliberate or accidental overdosage, treat symptoms on appearance. There are no special procedures recommended.

5. Pharmacological Properties 5.1 Pharmacodynamic Properties

Physiologically simeticone is extremely inert, and therefore it will not be pharmacologically active.

5.2 Pharmacokinetic Properties

Simeticone (activated dimeticone) is not absorbed following oral administration. It acts by changing the surface tension of gas bubbles, causing them to coalesce.

5.3 Preclinical Safety Data

Simeticone is physiologically inert and considered to be non-toxic. It is not absorbed following oral administration, nor is it pharmacologically active. Preclinical data reveal no hazard for humans.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Dextrates (hydrated) USNF

Sorbitol Crystalline EP

Tribasic Calcium Phosphate (Powder) USNF

Citric Acid Anhydrous (Powder) EP

Natural and artificial peppermint flavour No. 517

(Spray dried) HSE

Talc (purified) EP

Non-pareil seeds (Starch/Sucrose) HSE

6.2 Incompatibilities

None known.

6.3 Shelf Life

3 years in PVC/PVDC Al foil blister packs. 3 years in PVC/PE/Aclar Al. foil blister packs.

6.4 Special Precautions For Storage

Store below 25oC.

Store in a dry place.

6.5 Nature And Contents Of Container

Blister packs of construction 190 ?m PVC (product contact side)/51?m PE/38?m aclar and 25?m aluminium foil with vinyl sealing coat (product contact side).

or

Blister packs of construction 250?m PVC (product contact side)/PVDC 60 g/m2 and 20 ?m aluminium foil with vinyl heat sealing coat (product contact side).

Pack sizes: 4, 10, 20, 30, 50.

6.6 Special Precautions For Disposal And Other Handling

Not applicable.

7. Marketing Authorisation Holder

Stafford-Miller Limited

980 Great West Road

Brentford

Middlesex

TW8 9GS

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

8. Marketing Authorisation Number(S)

PL 00036/0084

9. Date Of First Authorisation/Renewal Of The Authorisation

25th May 2001

10. Date Of Revision Of The Text

February 2008


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Leader All Day Allergy


cetirizine hydrochloride
Dosage Form: tablet
Cardinal Health All Day Allergy Tablets Drug Facts Active ingredient (in each tablet)

Cetirizine HCl 10 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

runny nose sneezing itchy, watery eyes itching of the nose or throat Warnings Do not use

if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives.

When using this product drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding: if breast-feeding: not recommended if pregnant: ask a health professional before use. Keep out of reach of children.

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

Directions

adults and children

6 years and over one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms. adults 65 years and over ask a doctor children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other information do not use if blister unit is broken or torn (Blister Only) store between 20° to 25°C (68° to 77°F) Inactive ingredients

corn starch, FD&C blue no. 1, hypromellose, lactose, magnesium stearate, polydextrose, polyethylene glycol, povidone, titanium dioxide, triacetin

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Zyrtec® active ingredient

Indoor & Outdoor Allergies

Original Prescription Strength

All Day Allergy

Cetirizine Hydrochloride Tablets, 10 mg

Antihistamine

24 Hour Relief of:

Sneezing

Runny Nose

Itchy Throat or Nose

Itchy, Watery Eyes

Actual Size

All Day Allergy Tablets Carton


Leader All Day Allergy 
cetirizine hydrochloride  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 37205-825 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (CETIRIZINE) CETIRIZINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE Score no score Shape OVAL Size 10mm Flavor Imprint Code 4H2 Contains          Packaging # NDC Package Description Multilevel Packaging 1 37205-825-74 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 14 TABLET In 1 BLISTER PACK This package is contained within the CARTON (37205-825-74) 2 37205-825-65 1 BOTTLE In 1 PACKAGE contains a BOTTLE 2 30 TABLET In 1 BOTTLE This package is contained within the PACKAGE (37205-825-65) 3 37205-825-75 1 BOTTLE In 1 PACKAGE contains a BOTTLE 3 90 TABLET In 1 BOTTLE This package is contained within the PACKAGE (37205-825-75) 4 37205-825-70 1 BOTTLE In 1 PACKAGE contains a BOTTLE 4 45 TABLET In 1 BOTTLE This package is contained within the PACKAGE (37205-825-70)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078336 01/16/2008
Labeler - Cardinal Health (097537435) Revised: 05/2009Cardinal Health
More Leader All Day Allergy resources Leader All Day Allergy Side Effects (in more detail) Leader All Day Allergy Dosage Leader All Day Allergy Use in Pregnancy & Breastfeeding Leader All Day Allergy Drug Interactions Leader All Day Allergy Support Group 1 Review for Leader All Day Allergy - Add your own review/rating Compare Leader All Day Allergy with other medications Hay Fever Urticaria
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Topcare Allergy Relief 24 Hour


Generic Name: loratadine
Dosage Form: tablet
Topco Allergy Relief Drug Facts Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

runny nose sneezing itchy, watery eyes itching of the nose or throat Warnings Do not use

if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product

do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other information do not use if blister unit is broken or torn (Blister Only) do not use if printed foil under cap is broken or missing (Bottle Only) store at 20°-25°C (68°-77°F) protect from excessive moisture (Blister Only) Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-888-423-0139

Principal Display Panel

Original Prescription Strength

Non-Drowsy*

24 Hour

*When taken as directed. See Drug Facts Panel.

Allergy Relief

Loratadine Tablets, 10 mg/Antihistamine

Indoor & Outdoor Allergies

For 24 Hour Relief of:

Sneezing, Itchy, Watery Eyes, Runny Nose, Itchy Throat or Nose

Actual Size

Compare to Claritin® active ingredient

Allergy Relief Carton


TOPCARE ALLERGY RELIEF  24 HOUR
loratadine  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 36800-612 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (LORATADINE) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE Score no score Shape OVAL Size 8mm Flavor Imprint Code L612 Contains          Packaging # NDC Package Description Multilevel Packaging 1 36800-612-65 1 BOTTLE In 1 CARTON contains a BOTTLE 1 30 TABLET In 1 BOTTLE This package is contained within the CARTON (36800-612-65) 2 36800-612-72 1 BOTTLE In 1 CARTON contains a BOTTLE 2 60 TABLET In 1 BOTTLE This package is contained within the CARTON (36800-612-72) 3 36800-612-76 1 BOTTLE In 1 CARTON contains a BOTTLE 3 120 TABLET In 1 BOTTLE This package is contained within the CARTON (36800-612-76) 4 36800-612-87 1 BOTTLE In 1 CARTON contains a BOTTLE 4 300 TABLET In 1 BOTTLE This package is contained within the CARTON (36800-612-87) 5 36800-612-46 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 5 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (36800-612-46)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076301 01/25/2005
Labeler - Topco Associates LLC (006935977) Revised: 09/2009Topco Associates LLC
More Topcare Allergy Relief 24 Hour resources Topcare Allergy Relief 24 Hour Side Effects (in more detail) Topcare Allergy Relief 24 Hour Use in Pregnancy & Breastfeeding Drug Images Topcare Allergy Relief 24 Hour Drug Interactions Topcare Allergy Relief 24 Hour Support Group 21 Reviews for Topcare Allergy Relief 24 Hour - Add your own review/rating Compare Topcare Allergy Relief 24 Hour with other medications Hay Fever Urticaria
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Nighttime Sleepaid



Dosage Form: tablet
CVS Pharmacy, Inc. Nighttime Sleep Aid Tablets Drug Facts Active ingredient (in each tablet)

Doxylamine succinate 25 mg

Purpose

Nighttime sleep-aid

Uses helps to reduce difficulty in falling asleep Warnings

Ask a doctor before use if you have

a breathing problem such as asthma, emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland Do not give

to children under 12 years of age

Ask a doctor or pharmacist before use if you are

taking any other drugs

When using this product avoid alcoholic beverages take only at bedtime Stop use and ask a doctor if sleeplessness persists continuously for more than two weeks. Insomnia may be a symptom of serious underlying medical illness. If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 12 years of age and over: take one tablet 30 minutes before going to bed; take once daily or as directed by a doctor children under 12 years of age: do not use Other information store at 68°-77°F (20°-25°C) retain in carton until time of use see carton end panel for lot number and expiration date Inactive ingredients

dibasic calcium phosphate, FD&C blue no. 1 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to the active ingredient in Unisom® SleepTabs®

Nighttime

Sleep Aid

Doxylamine Succinate Tablets, 25 mg USP

Nighttime Sleep Aid

Fall Asleep Fast

Safe. Proven Effective

Just One Tablet Per Dose

Actual Size

Nighttime Sleep Aid Tablets Carton


NIGHTTIME SLEEP AID 
doxylamine succinate  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 59779-441 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOXYLAMINE SUCCINATE (DOXYLAMINE) DOXYLAMINE SUCCINATE 25 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color BLUE Score no score Shape OVAL Size 10mm Flavor Imprint Code L441 Contains          Packaging # NDC Package Description Multilevel Packaging 1 59779-441-64 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 16 TABLET In 1 BLISTER PACK This package is contained within the CARTON (59779-441-64)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA040167 07/23/1997
Labeler - CVS Pharmacy (062312574) Revised: 06/2009CVS Pharmacy
More Nighttime Sleepaid resources Nighttime Sleepaid Side Effects (in more detail)Nighttime Sleepaid Use in Pregnancy & BreastfeedingDrug ImagesNighttime Sleepaid Drug InteractionsNighttime Sleepaid Support Group8 Reviews for Nighttime Sleepaid - Add your own review/rating Compare Nighttime Sleepaid with other medications AllergiesConjunctivitis, AllergicHay FeverInsomniaNasal CongestionRhinorrheaUpper Respiratory Tract Infection
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Care One Sleep Aid


doxylamine succinate
Dosage Form: tablet
American Sales Company Sleep Aid Tablets Drug Facts Active ingredient (in each tablet)

Doxylamine succinate 25 mg

Purpose

Nighttime sleep-aid

Uses helps to reduce difficulty in falling asleep Warnings

Ask a doctor before use if you have

a breathing problem such as asthma, emphysema or chronic bronchitis glaucoma trouble urinating due to an enlarged prostate gland Do not give

to children under 12 years of age

Ask a doctor or pharmacist before use if you are

taking any other drugs

When using this product avoid alcoholic beverages take only at bedtime Stop use and ask a doctor if sleeplessness persists continuously for more than two weeks. Insomnia may be a symptom of serious underlying medical illness. If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 12 years of age and over: take one tablet 30 minutes before going to bed; take once daily or as directed by a doctor children under 12 years of age: do not use Other information store at 68°-77°F (20°-25°C) retain in carton until time of use see carton end panel for lot number and expiration date Inactive ingredients

dibasic calcium phosphate, FD&C blue no. 1 aluminum lake, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

1-800-719-9260

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Compare to the Active Ingredient in Unisom® SleepTabs®

Fall Asleep Fast!

Sleep Aid

Doxylamine Succinate Tablets, 25 mg

Nighttime Sleep-Aid

Safe, Proven Effective.

Just One Tablet Per Dose

Actual Size

Sleep Aid Tablets Carton


Care One Sleep Aid 
doxylamine succinate  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 41520-441 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOXYLAMINE SUCCINATE (DOXYLAMINE) DOXYLAMINE SUCCINATE 25 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color BLUE Score no score Shape OVAL Size 10mm Flavor Imprint Code L441 Contains          Packaging # NDC Package Description Multilevel Packaging 1 41520-441-64 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 16 TABLET In 1 BLISTER PACK This package is contained within the CARTON (41520-441-64)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA040167 06/29/2004
Labeler - American Sales Company (809183973) Revised: 06/2009American Sales Company
More Care One Sleep Aid resources Care One Sleep Aid Dosage Care One Sleep Aid Use in Pregnancy & Breastfeeding Care One Sleep Aid Drug Interactions 0 Reviews for Care One Sleep Aid - Add your own review/rating Compare Care One Sleep Aid with other medications Allergies Conjunctivitis, Allergic Hay Fever Insomnia Nasal Congestion Rhinorrhea Upper Respiratory Tract Infection
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Wal-Zyr D


cetirizine hydrochloride and pseudoephedrine hydrochloride
Dosage Form: tablet, extended release
Walgreen Co. Wal-Zyr™ D Drug Facts Active ingredient (in each extended release tablet)

Cetirizine HCl 5 mg

Pseudoephedrine HCl 120 mg

Purpose

Antihistamine

Nasal Decongestant

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat nasal congestion reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine. if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have heart disease thyroid disease diabetes glaucoma high blood pressure trouble urinating due to an enlarged prostate gland liver or kidney disease. Your doctor should determine if you need a different dose. Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives.

When using this product do not use more than directed drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. you get nervous, dizzy, or sleepless symptoms do not improve within 7 days or are accompanied by fever If pregnant or breast-feeding: if breast-feeding: not recommended if pregnant: ask a health professional before use. Keep out of reach of children.

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


Directions do not break or chew tablet; swallow tablet whole adults and children 12 years and over take 1 tablet every 12 hours; do not take more than 2 tablets in 24 hours. adults 65 years and over ask a doctor children under 12 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other information store between 20° to 25°C (68° to 77°F) Inactive ingredients

colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, talc, yellow iron oxide

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Zyrtec-D® active ingredients

Wal-Zyr™ D

Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride Extended Release Tablets, 5mg/120mg

antihistamine/nasal decongestant

Allergy & Congestion

Indoor & Outdoor Allergies

12 Hour

12 Hour Relief of:

Sneezing

Itchy, Watery Eyes

Runny Nose

Itchy Throat or Nose

Sinus Pressure

Nasal Congestion

Actual Size

Tablets

Wal-Zyr(tm) D Carton


WAL ZYR D  ALLERGY AND CONGESTION
cetirizine hcl, pseudoephedrine hcl  tablet, extended release Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0363-0176 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (CETIRIZINE) CETIRIZINE HYDROCHLORIDE 5 mg PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE (one side white one side light yellow) Score no score Shape ROUND Size 12mm Flavor Imprint Code 5029;5;120 Contains          Packaging # NDC Package Description Multilevel Packaging 1 0363-0176-53 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (0363-0176-53) 2 0363-0176-62 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (0363-0176-62)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077170 04/10/2008
Labeler - Walgreen Company (008965063) Revised: 06/2009Walgreen Company
More Wal-Zyr D resources Wal-Zyr D Side Effects (in more detail) Wal-Zyr D Dosage Wal-Zyr D Use in Pregnancy & Breastfeeding Wal-Zyr D Drug Interactions 0 Reviews for Wal-Zyr D - Add your own review/rating All Day Allergy-D Concise Consumer Information (Cerner Multum) Zyrtec-D Advanced Consumer (Micromedex) - Includes Dosage Information Compare Wal-Zyr D with other medications Hay Fever
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Sinus 12 Hour Drug Facts


Generic Name: pseudoephedrine hydrochloride
Dosage Form: tablet, film coated, extended release
McKesson Sinus 12 Hour Drug Facts Active ingredient (in each tablet)

Pseudoephedrine HCl 120 mg

Purpose

Nasal decongestant

Uses temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies, and nasal congestion associated with sinusitis temporarily relieves sinus congestion and pressure Warnings

Do not use

if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have high blood pressure heart disease diabetes thyroid disease trouble urinating due to an enlarged prostate gland When using this product do not use more than directed Stop use and ask a doctor if you get nervous, dizzy, or sleepless symptoms do not improve within 7 days or are accompanied by fever If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 12 years of age and over: one tablet every 12 hours not to exceed two tablets in 24 hours children under 12 years of age: use of product not recommended Other information each tablet contains: calcium 45 mg store at 20° - 25°C (68° - 77°F) in a dry place protect from light do not use if blister unit is broken or torn see carton end panel for lot number and expiration date this product meets the requirements of USP Drug Release Test 3 Inactive ingredients

carnauba wax, colloidal silicon dioxide, dibasic calcium phosphate, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, titanium dioxide

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Sudafed® 12 Hour Active Ingredient

Sinus 12 Hour

Pseudoephedrine Hydrochloride Extended-Release Tablets, 120 mg

Long-Acting Nasal Decongestant

Maximum Strength

Nasal & Sinus Congestion due to Colds & Allergies

Sinus Pressure

Non-Drowsy

120 mg each

*Capsule-Shaped Tablets


Sinus 12 Hour Carton


SUN MARK SINUS  12 HOUR
pseudoephedrine hydrochloride  tablet, film coated, extended release Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 49348-361 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE Score no score Shape CAPSULE Size 18mm Flavor Imprint Code L054 Contains          Packaging # NDC Package Description Multilevel Packaging 1 49348-361-01 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (49348-361-01)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA075153 06/24/2003
Labeler - McKesson (177667227) Revised: 08/2009McKesson
More Sinus 12 Hour Drug Facts resources Sinus 12 Hour Drug Facts Side Effects (in more detail) Sinus 12 Hour Drug Facts Use in Pregnancy & Breastfeeding Drug Images Sinus 12 Hour Drug Facts Drug Interactions Sinus 12 Hour Drug Facts Support Group 8 Reviews for Sinus2 Hour Drug Facts - Add your own review/rating Compare Sinus 12 Hour Drug Facts with other medications Nasal Congestion
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Cetiri D


cetirizine hydrochloride and pseudoephedrine hydrochloride
Dosage Form: tablet, extended release
Rite Aid Corporation Cetiri-D Drug Facts Active ingredient (in each extended release tablet)

Cetirizine HCl 5 mg

Pseudoephedrine HCl 120 mg

Purpose

Antihistamine

Nasal Decongestant

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat nasal congestion reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine. if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have heart disease thyroid disease diabetes glaucoma high blood pressure trouble urinating due to an enlarged prostate gland liver or kidney disease. Your doctor should determine if you need a different dose. Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives.

When using this product do not use more than directed drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. you get nervous, dizzy, or sleepless symptoms do not improve within 7 days or are accompanied by fever If pregnant or breast-feeding: if breast-feeding: not recommended if pregnant: ask a health professional before use. Keep out of reach of children.

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


Directions do not break or chew tablet; swallow tablet whole adults and children 12 years and over take 1 tablet every 12 hours; do not take more than 2 tablets in 24 hours. adults 65 years and over ask a doctor children under 12 years of age ask a doctor consumers with liver or kidney disease ask a doctor Other information store between 20° to 25°C (68° to 77°F) Inactive ingredients

colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, talc, yellow iron oxide

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to the Active Ingredients of Zyrtec-D®

Original Prescription Strength

Cetiri-D

Cetirizine Hydrochloride and

Pseudoephedrine Hydrochloride

Extended Release Tablets

5 mg/120 mg

antihistamine/nasal decongestant

Allergy & Congestion

Indoor & Outdoor Allergies

Actual Size

12 Hour

12 Hour Relief Of

Sneezing

Itchy, Watery Eyes

Runny Nose

Itchy Throat or Nose

Sinus Pressure

Nasal Congestion

Cetiri-D Carton


Cetiri D 
cetirizine hcl, pseudoephedrine hcl  tablet, extended release Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 11822-0176 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (CETIRIZINE) CETIRIZINE HYDROCHLORIDE 5 mg PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE (one side white one side light yellow) Score no score Shape ROUND Size 12mm Flavor Imprint Code 5029;5;120 Contains          Packaging # NDC Package Description Multilevel Packaging 1 11822-0176-1 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11822-0176-1) 2 11822-0176-2 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11822-0176-2)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077170 04/10/2008
Labeler - Rite Aid Corporation (014578892) Revised: 06/2009Rite Aid Corporation
More Cetiri D resources Cetiri D Side Effects (in more detail) Cetiri D Dosage Cetiri D Use in Pregnancy & Breastfeeding Cetiri D Drug Interactions Cetiri D Support Group 0 Reviews for Cetiri D - Add your own review/rating Compare Cetiri D with other medications Hay Fever
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Leader Allerhist


clemastine fumarate
Dosage Form: tablet
Cardinal Health Allerhist Drug Facts Active ingredient (in each tablet)

Clemastine fumarate, USP 1.34 mg (equivalent to 1 mg clemastine)

Purpose

Antihistamine

Uses

temporarily reduces these symptoms of the common cold, hay fever, and other respiratory allergies:

runny nose itchy, watery eyes sneezing itching of the nose or throat Warnings Ask a doctor before use if you have a breathing problem such as emphysema or chronic bronchitis glaucoma trouble urinating due to an enlargement of the prostate gland Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers

When using this product avoid alcoholic drinks drowsiness may occur alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery excitability may occur, especially in children If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions adults and children 12 years of age and over: take 1 tablet every 12 hours; not more than 2 tablets in 24 hours unless directed by a doctor children under 12 years of age: consult a doctor Other information sodium free store at 15°-30°C (59°-86°F) Inactive ingredients

colloidal silicon dioxide, lactose monohydrate, povidone, pregelatinized starch, starch, stearic acid

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Tavist® Allergy active ingredient

Allerhist

Clemastine Fumarate Tablets, USP 1.34 mg

Antihistamine

12 Hour Relief

Runny Nose

Sneezing

Itchy, Watery Eyes

Itchy Throat

Allerhist Carton


Leader Allerhist 
clemastine fumarate  tablet Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 37205-228 Route of Administration ORAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CLEMASTINE FUMARATE (CLEMASTINE) CLEMASTINE FUMARATE 1.34 mg Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found Product Characteristics Color WHITE (off white) Score 2 pieces Shape CAPSULE Size 9mm Flavor Imprint Code L282 Contains          Packaging # NDC Package Description Multilevel Packaging 1 37205-228-73 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 8 TABLET In 1 BLISTER PACK This package is contained within the CARTON (37205-228-73)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA074512 09/30/1997
Labeler - Cardinal Health (097537435) Revised: 08/2009Cardinal Health
More Leader Allerhist resources Leader Allerhist Side Effects (in more detail) Leader Allerhist Dosage Leader Allerhist Use in Pregnancy & Breastfeeding Leader Allerhist Drug Interactions 0 Reviews for Leader Allerhist - Add your own review/rating Compare Leader Allerhist with other medications Allergic Reactions Hay Fever Urticaria
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