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Aquadrate 10% w / w Cream


Aquadrate 10% w/w Cream

(Urea)

What is this leaflet about?

This leaflet is a summary of information about Aquadrate Cream. Read it carefully and keep it in case you need to refer to it again. If you have any questions about the cream, or your illness, ask your pharmacist (chemist) or doctor.

What is in Aquadrate Cream?

Aquadrate Cream contains the active ingredient Urea (10% w/w) and comes in tubes of 30g and 100g. Each 30g/100g tube contains 3g/10g of urea.

The cream also contains white soft paraffin, maize starch, isopropyl myristate, glyceryl tribehenate, palmitic acid, sorbitan laurate and polyoxyethylene fatty glyceride.

Who makes Aquadrate Cream?

The Marketing Authorisation holder is

Alliance Pharmaceuticals Ltd Avonbridge House Chippenham Wiltshire SN15 2BB England

and is licensed to sell Aquadrate Cream in the UK and Eire. It is made by

Laboratoires Chemineau Vouvray France What is Aquadrate Cream used for?

It is used to treat dry, scaly skin conditions. The urea in the cream helps to soften and moisturise your skin.

Is Aquadrate Cream right for you?

Tell your doctor if :

you are using any other medicines that are applied to the skin, as Aquadrate might affect the action of the other medicine. you have ever had a reaction to this cream or to any of its ingredients (these are listed above). you are pregnant or breastfeeding. the cream irritates your skin or there is no improvement in your condition. How to use Aquadrate Cream

The cream is for external use only and should only be applied to the skin. It should not be used on moist or broken skin. Application of Aquadrate Cream may cause skin irritation (redness, burning or itching). If you forget to use the cream on any occasion, do not worry, just continue as normal.

Adults, Children and the Elderly:-

Wash affected areas well, rinse off all traces of soap, dry and apply a small amount of the cream twice daily. Your doctor may tell you to cover this with a special "occlusive" dressing, but this is not usually necessary.

Does Aquadrate Cream have side effects?

If used correctly, as directed by your doctor, the cream is unlikely to cause side effects.

Some people experience irritation when they apply the cream. If you notice this or any other unusual effect, tell your doctor.

Storing Aquadrate Cream

Keep all medicines out of the reach and sight of children and do not store above 30°C.

Do not use after the expiry date shown on the base of the tube.

PL Number 16853/0061

PA Number: 943/5/1

Legal category: P

This leaflet was last revised in May 2006

Aquadrate is a registered Trade mark

©Alliance Pharmaceuticals, Limited

AN 0729 004


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Topicort Ointment



Dosage Form: ointment
Topicort®
(Desoximetasone Ointment USP) 0.05%

For topical use only. Not for oral, ophthalmic, or intravaginal use.

Rx only

Topicort Ointment Description

Topicort® (desoximetasone ointment USP) 0.05% contains the active synthetic corticosteroid desoximetasone. The topical corticosteroids constitute a class of primarily synthetic steroids used as anti-inflammatory and antipruritic agents.

Each gram of Topicort® (desoximetasone ointment USP) 0.05% contains 0.5 mg of desoximetasone in an ointment base consisting of mineral oil and white petrolatum.

The chemical name of desoximetasone is Pregna-1, 4-diene-3, 20-dione, 9-fluoro-11, 21-dihydroxy- 16-methyl-,(11?,16?)-.

Desoximetasone has the molecular formula C22H29FO4 and a molecular weight of 376.47. The CAS Registry Number is 382-67-2.

The structural formula is:

Topicort Ointment - Clinical Pharmacology

Topical corticosteroids share anti-inflammatory, antipruritic and vasoconstrictive actions.

The mechanism of anti-inflammatory activity of the topical corticosteroids is unclear. Various laboratory methods, including vasoconstrictor assays, are used to compare and predict potencies and/or clinical efficacies of the topical corticosteroids. There is some evidence to suggest that a recognizable correlation exists between vasoconstrictor potency and therapeutic efficacy in man.

Pharmacokinetics

The extent of percutaneous absorption of topical corticosteroids is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings.

Topical corticosteroids can be absorbed from normal intact skin. Inflammation and/or other disease processes in the skin increase percutaneous absorption. Occlusive dressings substantially increase the percutaneous absorption of topical corticosteroids. Thus, occlusive dressings may be a valuable therapeutic adjunct for treatment of resistant dermatoses.

Once absorbed through the skin, topical corticosteroids are handled through pharmacokinetic pathways similar to systemically administered corticosteroids. Corticosteroids are bound to plasma proteins in varying degrees. Corticosteroids are metabolized primarily in the liver and are then excreted by the kidneys. Some of the topical corticosteroids and their metabolites are also excreted into the bile.

Pharmacokinetic studies in men with Topicort® (desoximetasone) Ointment 0.25% with tagged desoximetasone showed no detectable level (limit of sensitivity: 0.003 µg/mL) in 1 subject and 0.004 and 0.006 µg/mL in the remaining 2 subjects in the blood when it was applied topically on the back followed by occlusion for 24 hours. The extent of absorption for the ointment was 7% based on radioactivity recovered from urine and feces. Seven days after application, no further radioactivity was detected in urine or feces. Studies with other similarly structured steroids have shown that predominant metabolite reaction occurs through conjugation to form the glucuronide and sulfate ester.

Indications and Usage for Topicort Ointment

Topicort® (desoximetasone ointment USP) 0.05% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Contraindications

Topical corticosteroids are contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

Warnings

Keep out of reach of children.

Precautions General

Systemic absorption of topical corticosteroids can produce reversible hypothalamic-pituitary-adrenal (HPA) axis suppression with the potential for clinical glucocorticosteroid insufficiency. This may occur during treatment or upon withdrawal of the topical corticosteroid.

Because of the potential for systemic absorption, use of topical corticosteroids may require that patients be periodically evaluated for HPA axis suppression. Factors that predispose a patient using a topical corticosteroid to HPA axis suppression include the use of more potent steroids, use over large surface areas, use over prolonged periods, use under occlusion, use on an altered skin barrier, and use in patients with liver failure.

An ACTH stimulation test may be helpful in evaluating patients for HPA axis suppression. If HPA axis suppression is documented, an attempt should be made to gradually withdraw the drug, to reduce the frequency of application, or to substitute a less potent steroid. Manifestations of adrenal insufficiency may require supplemental systemic corticosteroids. Recovery of HPA axis function is generally prompt and complete upon discontinuation of topical corticosteroids.

Cushing's syndrome, hyperglycemia, and unmasking of latent diabetes mellitus can also result from systemic absorption of topical corticosteroids.

Use of more than one corticosteroid-containing product at the same time may increase the total systemic corticosteroid exposure.

Pediatric patients may be more susceptible to systemic toxicity from use of topical corticosteroids.

Local Adverse Reactions with Topical Corticosteroids

Local adverse reactions may be more likely to occur with occlusive use, prolonged use or use of higher potency corticosteroids. Reactions may include atrophy, striae, telangiectasias, burning, itching, irritation, dryness, folliculitis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, and miliaria. Some local adverse reactions may be irreversible.

Allergic Contact Dermatitis with Topical Corticosteroids

Allergic contact dermatitis to any component of topical corticosteroids is usually diagnosed by a failure to heal rather than a clinical exacerbation. Clinical diagnosis of allergic contact dermatitis can be confirmed by patch testing.

Concomitant Skin Infections

Concomitant skin infections should be treated with an appropriate antimicrobial agent. If the infection persists, Topicort® (desoximetasone ointment USP) 0.05% should be discontinued until the infection has been adequately treated.

Information for the Patient

Patients using topical corticosteroids should receive the following information and instructions:

This medication is to be used as directed by the physician. It is for external use only. Avoid contact with the eyes. Patients should be advised not to use this medication for any disorder other than that for which it was prescribed. The treated skin area should not be bandaged or otherwise covered or wrapped so as to be occlusive unless directed by the physician. Patients should report any signs of local adverse reactions, especially under occlusive dressings. Other corticosteroid-containing products should not be used with Topicort® (desoximetasone ointment USP) 0.05% without first consulting with the physician.

As with other corticosteroids, therapy should be discontinued when control is achieved. If no improvement is seen within 4 weeks, contact the physician.

Laboratory Tests

The following tests may be helpful in evaluating the hypothalamic-pituitary-adrenal (HPA) axis suppression:

  Urinary free cortisol test   ACTH stimulation test Carcinogenesis, Mutagenesis, and Impairment of Fertility

Long-term animal studies have not been performed to evaluate the carcinogenic potential or the effect on fertility of topical corticosteroids.

Desoximetasone was nonmutagenic in the Ames test.

Pregnancy Teratogenic Effects Pregnancy Category C

Corticosteroids have been shown to be teratogenic in laboratory animals when administered systemically at relatively low dosage levels. Some corticosteroids have been shown to be teratogenic after dermal application in laboratory animals.

Desoximetasone has been shown to be teratogenic and embryotoxic in mice, rats, and rabbits when given by subcutaneous or dermal routes of administration in doses 15 to 150 times the human dose of Topicort® (desoximetasone ointment USP) 0.05%.

There are no adequate and well-controlled studies in pregnant women on teratogenic effects from topically applied corticosteroids. Therefore, Topicort® (desoximetasone ointment USP) 0.05% should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Drugs of this class should not be used extensively on pregnant patients, in large amounts, or for prolonged periods of time.

Nursing Mothers

It is not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in breast milk. Systemically administered corticosteroids are secreted into breast milk in quantities not likely to have a deleterious effect on the infant. Nevertheless, caution should be exercised when topical corticosteroids are administered to a nursing woman.

Pediatric Use

Pediatric patients may demonstrate greater susceptibility to topical corticosteroid-induced HPA axis suppression and Cushing's syndrome than mature patients because of a larger skin surface area to body weight ratio.

Hypothalamic-pituitary-adrenal (HPA) axis suppression, Cushing's syndrome, and intracranial hypertension have been reported in pediatric patients receiving topical corticosteroids. Manifestations of adrenal suppression in pediatric patients include linear growth retardation, delayed weight gain, low plasma cortisol levels, and absence of response to ACTH stimulation. Manifestations of intracranial hypertension include bulging fontanelles, headaches, and bilateral papilledema.

Administration of topical corticosteroids to pediatric patients should be limited to the least amount compatible with an effective therapeutic regimen. Chronic corticosteroid therapy may interfere with the growth and development of pediatric patients.

Adverse Reactions

The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximate decreasing order of occurrence:

Burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, and miliaria.

In controlled clinical studies the incidence of adverse reactions was low (0.2%) for Topicort® (desoximetasone ointment USP) 0.05% and included mild burning sensation at the site of application.

Overdosage

Topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects (see PRECAUTIONS).

Topicort Ointment Dosage and Administration

Apply a thin film of Topicort® (desoximetasone ointment USP) 0.05% to the affected skin areas twice daily. Rub in gently.

How is Topicort Ointment Supplied

Topicort® (desoximetasone ointment USP) 0.05% is supplied in:

15 gram tubes (NDC 51672-5263-1) and 60 gram tubes (NDC 51672-5263-3).

Store at controlled room temperature between 20° to 25°C (68° to 77°F), excursions permitted to 15° to 30°C (59° to 86°F). [See USP Controlled Room Temperature]

Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1

Dist. by: TaroPharma a division of Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532

Topicort® and TaroPharma® are registered trademarks of Taro Pharmaceuticals U.S.A., Inc. and/or its affiliates.

Issued: November, 2010

PK-6692-0 83

PRINCIPAL DISPLAY PANEL - 15 g Tube Carton

NDC 51672-5263-1

15 g

Rx only

0.05%

OINTMENT

Topicort®
Desoximetasone Ointment USP, 0.05%
FOR TOPICAL USE ONLY. NOT FOR ORAL, OPHTHALMIC, OR INTRAVAGINAL USE.

Keep this and all medications out of the reach of children.

TaroPharma®


TOPICORT 
desoximetasone  ointment Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 51672-5263 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Desoximetasone (Desoximetasone) Desoximetasone 0.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength mineral oil   petrolatum   Product Characteristics Color WHITE (off-white) Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 51672-5263-5 10 TUBE In 1 CARTON contains a TUBE 1 5 g In 1 TUBE This package is contained within the CARTON (51672-5263-5) 2 51672-5263-1 1 TUBE In 1 CARTON contains a TUBE 2 15 g In 1 TUBE This package is contained within the CARTON (51672-5263-1) 3 51672-5263-3 1 TUBE In 1 CARTON contains a TUBE 3 60 g In 1 TUBE This package is contained within the CARTON (51672-5263-3)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA018594 01/17/1985
Labeler - Taro Pharmaceuticals U.S.A., Inc. (145186370) Establishment Name Address ID/FEI Operations Taro Pharmaceuticals Inc. 206263295 MANUFACTURE Revised: 12/2010Taro Pharmaceuticals U.S.A., Inc. More Topicort Ointment resources Topicort Ointment Side Effects (in more detail) Topicort Ointment Use in Pregnancy & Breastfeeding Topicort Ointment Drug Interactions Topicort Ointment Support Group 9 Reviews for Topicort - Add your own review/rating Compare Topicort Ointment with other medications Atopic Dermatitis Dermatitis Eczema Psoriasis
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Skin Cancer Medications


Definition of Skin Cancer:

Skin cancer is the uncontrolled growth of skin cells. If left unchecked, these cancer cells can spread from the skin into other tissues and organs.

There are different types of skin cancer. Basal cell carncinoma is the most common. Melanoma is less common, but more dangerous.

Drugs associated with Skin Cancer

The following drugs and medications are in some way related to, or used in the treatment of Skin Cancer. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

Topics under Skin Cancer Basal Cell Carcinoma (6 drugs) Melanoma (16 drugs in 2 topics) Squamous Cell Carcinoma (2 drugs) Learn more about Skin Cancer

Micromedex Care Notes:

Liposarcoma Squamous Cell Carcinoma

Medical Encyclopedia:

Skin cancer

Drugs.com Health Center:

Skin Cancer
Drug List: Carac-Cream Efudex-Cream Efudex-Occlusion-Pack Fluoroplex-Cream
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Aphthous Stomatitis, Recurrent Medications


Drugs associated with Aphthous Stomatitis, Recurrent

The following drugs and medications are in some way related to, or used in the treatment of Aphthous Stomatitis, Recurrent. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.


Drug List: Ala-Cort Ala-Scalp-Hp Anucort-Hc-Cream-Ointment-Suppository Anumed-Hc-Cream-Ointment-Suppository Aphthasol Aquanil-Hc Beta-Hc Caldecort Cetacort Cortaid Cortaid-Intensive-Therapy Cortaid-Maximum-Strength Cortaid-With-Aloe Cortalo-With-Aloe Corticaine Cortizone-For-Kids Cortizone-10-Cream Cortizone-10-Anal-Itch-Cream-Cream-Ointment-Suppository Cortizone-10-Intensive-Healing-Formula Cortizone-10-Plus Cortizone-5 Cotacort Dermarest-Dricort Dermarest-Eczema-Medicated Dermarest-Plus-Anti-Itch Dermtex-Hc Genasone-Aloe Gly-Cort Gynecort-Maximum-Strength Hemorrhoidal-Hc-Cream-Ointment-Suppository Hemril-30-Cream-Ointment-Suppository Hemril-Hc-Uniserts-Cream-Ointment-Suppository Hycort Hydrocortisone-1-In-Absorbase Hydrocortisone-With-Aloe-Cream Hytone-Cream Instacort-Gel Itch-X-Foam Lacticare-Hc Locoid-Cream Locoid-Lipocream Massengill-Medicated-Soft-Cloth Md-Hydrocortisone Neutrogena-T-Scalp Nucort-With-Aloe Nutracort-Lotion Nuzon Pandel Pediaderm-Hc-Lotion Procto-Kit-1-Cream-Ointment-Suppository Procto-Kit-2-5-Cream-Ointment-Suppository Procto-Pak-1-Cream-Ointment-Suppository Proctocare-Hc-Cream Proctocort-Cream-Ointment-Suppository Proctocream-Hc-Cream-Ointment-Suppository Proctosert-Hc-Cream-Ointment-Suppository Proctosol-Hc-Cream-Ointment-Suppository Proctozone-Hc-Cream-Ointment-Suppository Proctozone-H-Cream-Ointment-Suppository Recort-Plus Rectasol-Hc-Cream-Ointment-Suppository Rederm Sarnol-Hc Scalacort Scalpcort Scalpicin-Gel Texacort U-Cort Westcort-Cream
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Topical antihistamines


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.

Topical antihistamine products are where antihistamines have been incorporated in creams, nasal sprays and other agents that can be applied locally (for example to the skin) to treat allergic reactions.

Antihistamines block the histamine receptors, which when activated cause allergic reactions such as hay fever, itching and rash. Topical antihistamines are used to relieve the symptoms of hay fever, itching and to resolve rashes due to allergy.

See also

Medical conditions associated with topical antihistamines:

Atopic Dermatitis Dermatitis Eczema Lichen Simplex Chronicus Pain Pruritus Drug List: Ivarest Derma-Pax-Lotion Dermarest-Cream Prudoxin-Topical Zonalon-Cream
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Boots Antifungal Cream


Boots Antifungal Cream

(Clotrimazole)

for fungal infections of the skin

20 g

Read all of this carton for full instructions.

What this medicine is for

An antifungal cream for the treatment of fungal skin infections including ringworm, athlete’s foot, fungal nappy rash, infections of the armpit, groin, toes and skin folds and thrush of the vulva or penis.

Before you use this medicine Do not use: If you are allergic to any of the ingredients If you are pregnant or breastfeeding, unless your doctor or midwife tells you to

Information about some of the ingredients: The ingredients in the cream may affect the latex used in contraceptives such as condoms and diaphragms. This may reduce the effectiveness of the contraceptives. You should therefore use other methods of contraception for at least 5 days after using this medicine in the genital area. You may, for example, use a spermicide gel in addition to the condom or diaphragm. If you need more advice about this speak to your pharmacist.

Cetyl alcohol and stearyl alcohol in this medicine may cause skin reactions (e.g. contact dermatitis).

How to use this medicine

Check the tube seal is not broken before first use. If it is, do not use the cream.

Pierce tube seal with end of cap.

Adults and children: Apply to the affected area two or three times a day. Use the cream for at least 2 weeks. In some cases it may be necessary to continue to use the cream for more than 4 weeks.

If you are using the cream for a foot infection, make sure your feet, especially between the toes, are washed and thoroughly dried before applying the cream. Apply to the skin only.

Do not use more than the amount recommended above.

If symptoms do not go away talk to your doctor.

If anyone accidentally swallows some: Talk to a doctor straight away.

Possible side effects

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

If you get these side effects, stop using the cream and see a doctor: Allergic reaction (e.g. skin rash, red or itchy skin) These other effects are less serious. If they bother you talk to a pharmacist: Rarely, mild burning or irritation immediately after using the cream Pain

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

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

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

Active ingredient

This topical cream contains Clotrimazole 1% w/w.

Also contains: purified water, 2-octyldodecanol, stearyl alcohol, cetyl alcohol, cetyl esters wax, sorbitan stearate, polysorbate 60, benzyl alcohol.

PL 10622/0004 [P]

Text prepared 8/08

Manufactured for The Boots Company PLC Nottingham NG2 3AA

by

Thornton & Ross Ltd Linthwaite Huddersfield West Yorkshire HD7 5QH Marketing Authorisation held by PLIVA Pharma Ltd Vision House Bedford Road Petersfield Hampshire GU32 2QB

If you need more advice ask your pharmacist.

1498cXPil


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Rosiced 7.5mg / g cream


ROSICED 7.5 mg/g Cream

Active substance: metronidazole

For adult use

Read all of this leaflet carefully before you start using this medicine. Keep this leaflet. You may need to read it again. If you have any further questions, ask your doctor or pharmacist. This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours. If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist. In this leaflet: 1. What ROSICED 7.5mg/g Cream is and what it is used for 2. Before you use ROSICED 7.5mg/g Cream 3. How to use ROSICED 7.5mg/g Cream 4. Possible side effects 5. How to store ROSICED 7.5mg/g Cream 6. Further information WHAT ROSICED 7.5mg/g Cream IS AND WHAT IT IS USED FOR

ROSICED 7.5mg/g Cream is used to treat inflammation caused by rosacea. Inflammatory rosacea is a skin condition that causes redness, papules (pink bumps) and pustules (pus-filled spots) on the face.

BEFORE YOU USE ROSICED 7.5mg/g Cream Do not use ROSICED 7.5mg/g Cream if you are allergic (hypersensitive) to metronidazole or any of the other ingredients of ROSICED 7.5mg/g Cream . All ingredients used in ROSICED 7.5mg/g Cream are listed in section 6 of this leaflet. If you are not sure whether you are allergic, please ask your doctor or pharmacist. if you are in the first 3 months of pregnancy.

If you have any of the following:

severe liver damage (e.g. cirrhosis of the liver), problems affecting blood formation (e.g. anaemia), diseases affecting the brain, bone marrow or nerves

please tell your doctor. In such cases, treatment with ROSICED 7.5mg/g Cream must be carefully considered.

Take special care with ROSICED 7.5mg/g Cream: when using it near the eyes or mucous membranes. Such contact should be avoided. If contact occurs, the cream should be washed away carefully with water. when exposing your skin to sunlight or ultraviolet (UV) light (e.g. sun beds or solarium visits). Avoid strong sunlight or UV light as metronidazole is not stable under UV light and it may lose its effectiveness, or its effectiveness may be altered. if you have, or have ever had, a blood condition (dyscrasia). A dyscrasia may manifest among other symptoms as a blood clotting disorder. Using ROSICED 7.5mg/g Cream with other medicines

Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.

To date, there are no known interactions with other drugs applied to the skin.

Pregnancy and breast-feeding

Ask your doctor or pharmacist for advice before taking any medicine.

Pregnancy

ROSICED 7.5mg/g Cream should not be used in the first three months of pregnancy. To be on the safe side, if you are not sure whether you are pregnant, you should undergo a pregnancy test. ROSICED 7.5mg/g Cream should only be used in the last six months of pregnancy if other treatments have proved ineffective.

Breast-feeding

Metronidazole (the active substance of ROSICED 7.5mg/g Cream) passes into breast milk.

During the breast-feeding period, you should either stop breast-feeding or refrain from using ROSICED 7.5mg/g Cream.

Children and adolescents

ROSICED 7.5mg/g Cream is not recommended for use in children.

As rosacea does not affect children, no trials have been performed on children with regard to safety and tolerability.

Driving and using machines

ROSICED 7.5mg/g Cream has no effect on the ability to drive vehicles.

Important information about some of the ingredients of ROSICED 7.5mg/g Cream

ROSICED 7.5mg/g Cream contains propylene glycol, which can cause skin irritations.

HOW TO USE ROSICED 7.5mg/g Cream

Always use ROSICED 7.5mg/g Cream exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

Always wash and dry your face gently before each application.

Non-comedogenic cosmetics (that do not clog pores and cause blackheads) and non-astringent cosmetics (that do not draw together or constrict skin and wound tissue e.g. styptic pen) may be used following application of the cream. If you are unsure, ask your doctor or pharmacist which cosmetics you can use.

How much and how often you should apply ROSICED 7.5mg/g Cream

Dosage and method of administration

Unless otherwise prescribed by your doctor, the usual dose is as follows:

Apply the cream as a thin film twice daily to the affected areas of the face and gently rub it in.

Please consult your doctor or pharmacist if you have the impression that the action of ROSICED 7.5mg/g Cream is too strong or too weak.

How long you should use ROSICED 7.5mg/g Cream

You should normally use ROSICED 7.5mg/g Cream for a period of 6 weeks. If necessary, treatment can be extended. If no clinical improvement is achieved, treatment should be discontinued.

If you use more ROSICED 7.5mg/g Cream than you should:

Overdosage is extremely unlikely. If necessary, the product should by removed by washing with warm water.

If you forget to use ROSICED 7.5mg/g Cream:

Do not increase the dose to make up for a forgotten dose. Simply carry on using ROSICED 7.5mg/g Cream at the dosage schedule prescribed by your doctor.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

Possible Side Effects

Like all medicines, ROSICED 7.5mg/g Cream can cause side effects, although not everybody gets them.

The evaluation of side effects is based on the following frequencies:

very common: more than 1 in 10 cases treated
common: fewer than 1 in 10, but more than 1 in 100 cases treated
uncommon: fewer than 1 in 100, but more than 1 in 1,000 cases treated
rare: fewer than 1 in 1,000, but more than 1 in 10,000 cases treated
very rare: fewer than 1 in 10,000 cases treated, including isolated reports

Common side effects include dry skin, inflammation and a burning sensation on the skin.

In rare cases, swelling of the face and neck, sudden itching, fainting and breathlessness can occur.

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

HOW TO STORE ROSICED 7.5mg/g Cream

Keep out of the reach and sight of children.

Do not use ROSICED 7.5mg/g Cream after the expiry date which is stated on the tube and carton after Exp. The expiry date refers to the last day of that month.

Storage conditions

Do not store above 25?C.

Storage once ROSICED 7.5mg/g Cream has been opened

The cream can be used for up to 28 days after opening.

Do not use ROSICED 7.5mg/g Cream if you notice that the tube is damaged.

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 ROSICED 7.5mg/g Cream contains

The active substance is: metronidazole. One gram of cream contains 7.5 mg of metronidazole.

The other ingredients are:

glyceryl monolaurate, glyceryl monomyristate, propylene glycol, citric acid anhydrous, sodium hydroxide, carbomers, purified water.

What ROSICED 7.5mg/g Cream looks like and contents of the pack

ROSICED 7.5mg/g Cream is available in synthetic (polyethylene) tubes containing 25 g, 30 g, 40 g and 50 g. Not all pack sizes may be marketed in all countries.

Marketing authorisation holder Pierre Fabre Dermatologie 45 place Abel Gance 92100 Boulogne France Manufacturer Bioglan AB PO Box 50310 S-202 13 Malm? Sweden

This leaflet was last approved in:

26/02/2008


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Vaginal anti-infectives


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.

Vaginal anti-infectives are available as creams, pessaries (tablets), gels or solutions to treat either bacterial or fungal vaginal infections. Vaginal antifungal products are used to treat vaginal thrush. Antibacterial vaginal products are used for bacterial infections such as bacterial vaginosis. Other products are used to manage irritation or minor soreness.

See also

Medical conditions associated with vaginal anti-infectives:

AcneBacterial VaginitisCutaneous CandidiasisFungal Infection ProphylaxisOral ThrushPerioral DermatitisRosaceaTinea CorporisTinea CrurisTinea PedisTinea VersicolorVaginal Yeast Infection Drug List:/tags/gyne-lotrimin-cream/
/tags/vandazole/
/tags/monistat-7-cream/
/tags/gynazole-1-cream/
/tags/metrogel-vaginal-gel/
/tags/clindamax-cream/
/tags/derma-gran-af-topical/
/tags/aloe-vesta/
/tags/avc/
/tags/betadine-cream/
/tags/canesten-topical/
/tags/clindacin-p/
/tags/clotrimazole-7/
/tags/desenex-spray/
/tags/fungicure-pump-spray/
/tags/fungoid-kit/
/tags/gyne-sulf/
/tags/micatin-cream/
/tags/micatin-foot-powder/
/tags/micatin-jock-itch/
/tags/micon-7/
/tags/minidyne-solution/
/tags/mitrazol/
/tags/monistat-1-combo-pack-cream/
/tags/mycelex-cream/
/tags/ony-clear/
/tags/polydine-solution/
/tags/secura-antifungal-topical/
/tags/terazol-3-suppositories/
/tags/tetterine-cream/
/tags/trysul/
/tags/v-v-s/

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Boots Bite & Sting Relief 2 Years Plus Antihistamine Cream


Boots Bite & Sting Relief 2 Years Plus Antihistamine Cream

(Mepyramine Maleate)

From 2 years

Relieves pain, itching and swelling

20 g e

Read all of this carton for full instructions.

What this medicine is for

A soothing antihistamine cream for the relief of pain, itching and swelling caused by insect bites and stings, and nettle stings.

Before you use this medicine X Do not use: If you are allergic to any of the ingredients or other antihistamines If you have eczema or other skin conditions If you are pregnant or breastfeeding, unless your doctor tells you to On broken skin, sunburnt skin or on large areas of skin

Cetostearyl alcohol and lanolin may cause skin reactions (e.g. contact dermatitis).

How to use this medicine

Check the tube seal is not broken before first use. If it is, do not use the cream. Pierce tube seal with end of cap.

Apply to the skin only.

Adults and children of 2 years and over:

Smooth a very small amount on the affected area. Use the cream 2 or 3 times a day, for a maximum of 3 days.

Do not use on children under 2 years.

If a rash develops, or the condition gets worse, stop using the cream.

If symptoms do not go away talk to your doctor.

! If anyone accidentally swallows some:

Talk to a doctor straight away.

Possible side effects

Most people will not have problems.

If you get these side effects stop using the cream and see a doctor.

Allergic reaction (e.g. skin rash, red or itchy skin, worsening of the condition you are treating)

If 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 ingredient

This cream contains Mepyramine Maleate 2% w/w.

Also contains: purified water, cetostearyl alcohol, white soft paraffin, liquid paraffin, cetomacrogol 1000, anhydrous hypoallergenic lanolin, sorbitan sesquioleate, sodium citrate, citric acid monohydrate.

PL 00014/0440

Text prepared 2/07

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

If you need more advice ask your pharmacist.

BTC14991 vD 15-06-07


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Boots Lip and Cold Sore Cream


Boots Lip and Cold Sore Cream

Relieves cracked lips and cold sores

5 g

Read all of this carton for full instructions.

What this medicine is for

An antibacterial and protective cream for cracked lips and cold sores.

You can use this medicine if you are pregnant or breastfeeding.

How to use this medicine

Adults and children: Use a very small amount on the affected area every hour, when you need to.

Apply to the skin only.

Do not use more than the amount recommended above.

If symptoms do not go away talk to your doctor.

If anyone accidentally swallows some: Talk to a doctor.

Possible side effects

Cetostearyl alcohol may cause skin reactions (e.g. contact dermatitis).

If this becomes severe, or you notice any side effect, please tell your pharmacist or doctor.

How to store this medicine

Store below 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

This cream contains Cetrimide 0.5% w/w, Chlorocresol 0.1% w/w, Dimeticone 9% w/w, Urea 1% w/w.

Also contains: deionised water, liquid paraffin, cetostearyl alcohol.

PL 30306/0028

Text prepared 8/07

Manufactured for The Boots Company PLC Nottingham NG2 3AA

by

CCS Clean Chemicals Sweden AB Borl?nge SE 78173 Sweden Marketing Authorisation held by Actavis Group PTC ehf Reykjv?kurvegi 76 – 78 220 Hafnarfjorur Iceland

If you need more advice ask your pharmacist .

2787bXPil


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Efudix 5% Cream


EFUDIX 5% Cream

Fluorouracil

Please read this leaflet carefully before you start to take your medicine. If you have any questions or are not sure about anything, ask your doctor or pharmacist.

What Is Efudix Cream?

Efudix Cream contains the active ingredient fluorouracil, which belongs to a group of medicines known as antimetabolites, at a concentration of 5%. It works by interfering with the growth of abnormal cells which are eventually destroyed. It also contains the inactive ingredients stearyl alcohol, white soft paraffin, polysorbate 60, propylene glycol, methyl parahydroxybenzoate (methyl paraben), propyl parahydroxybenzoate (propyl paraben) and purified water.

The cream is supplied in tubes of 20 g and 40 g.

The Product Licence/Authorisation for Efudix Cream is held by Meda Pharmaceuticals Ltd. Skyway House Parsonage Road Takeley Bishop’s Stortford CM22 6PU UK It is made by ICN Polfa Rzesz?w S.A. ul. Przemys?owa 2 35-959 Rzesz?w Poland What Is Efudix Cream Used For?

Efudix Cream is used to treat certain skin conditions caused by abnormal cell growth including different types of keratoses (a horny growth of the skin), keratocanthoma (a firm nodule on the skin), Bowen’s disease and some simple skin cancers.

When Must Efudix Cream Not Be Used? If you are pregnant or breast feeding. If you are allergic to Efudix Cream or any of its ingredients including parabens. It is not recommended for use by children. When Should You Be Extra Careful When Using Efudix Cream?

Make sure your doctor knows if you are using any other medicines you apply to the areas of skin being treated (e.g. creams and ointments), including ones bought by yourself without a prescription.

May Efudix Cream Be Used During Pregnancy Or While Breast Feeding?

You must not use Efudix Cream if you are pregnant, think you may be pregnant or are breast feeding.

It is important to tell your doctor if you are pregnant, think you may be pregnant or intend to become pregnant during treatment.

How Should Efudix Cream Be Used? Always use Efudix Cream as your doctor tells you to. It must only be used on the skin. Be careful if applying Efudix Cream around your eyelids, nose and lips and avoid any contact with the eyes or mouth.Wash your hands thoroughly after use. If somebody else is helping you to apply the cream, they should take precautions to avoid cream being absorbed through their skin. It is recommended that they should wear disposable surgical gloves, remove these after use and wash their hands thoroughly. It is not necessary for you to wear gloves as the intended treatment results in some of the cream being absorbed. The cream should be applied in a thin layer to the affected area once or twice daily or as your doctor advises. The total area of skin treated at any one time should not be more than 23x23 cm (500 cm square) or 9x9 inches. Your doctor should tell you if you need to apply a dressing to the treated skin. You will normally need to use the cream for at least three to four weeks.Your skin may appear to be worse after you start the treatment. This is to be expected and you should continue to apply the cream as directed. If your skin becomes much worse, or if you are worried, consult your doctor. After stopping treatment you may find that your skin takes one to two months to heal completely. If the cream is swallowed or someone else accidentally uses it, contact your doctor, pharmacist or nearest hospital straight away. If you miss a dose, apply it as soon as possible. However, if it is nearly time for your next dose, skip the missed dose and carry on as before. Do not apply a double dose. Do not change the prescribed dose yourself. If you think the effect of your medicine is too weak or strong, talk to your doctor. What Are The Possible Unwanted Effects Of Efudix Cream?

In addition to the beneficial effects of Efudix Cream it is possible that unwanted effects will occur during treatment even when it is used as directed.

The cream may sometimes cause redness and discomfort in the affected skin and surrounding healthy skin and skin allergy may develop. Occasionally sores will develop and you may feel some discomfort. Rarely, the sores are round, red and painful. If you are suffering severe discomfort, your doctor may be able to help. Whilst using Efudix your skin may become more sensitive to sunlight.To prevent this you should try to stay out of direct sunlight as much as possible whilst using the cream and do not use a sunlamp or sunbed.

If you are concerned about these or any other unwanted effects, talk to your doctor.

How Should Efudix Cream Be Stored? Keep this medicine out of reach and sight of children. Do not store above 30°C. This medicine should not be used after the date (EXP) printed on the pack. Return any leftover medicine to your pharmacist who will arrange for environment-friendly disposal. Only keep it if your doctor tells you to. Remember this medicine is for you. Only a doctor can prescribe it for you. Never give it to others. It may harm them even if their symptoms are the same as yours. Further Information

You can get more information on Efudix Cream from your doctor or pharmacist.

DATE OF PREPARATION

June 2009

P1EU02

562101V5140UK00


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Gynazole-1 Cream


Pronunciation: byoo-toe-KOE-na-zole
Generic Name: Butoconazole
Brand Name: Gynazole-1
Gynazole-1 Cream is used for:

Treating vaginal yeast infections.

Gynazole-1 Cream is an antifungal agent. It works by weakening the cell wall of sensitive fungi, causing the cell contents to leak. This kills the fungi.

Do NOT use Gynazole-1 Cream if: you are allergic to any ingredient in Gynazole-1 Cream

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

Before using Gynazole-1 Cream:

Some medical conditions may interact with Gynazole-1 Cream. 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

Some MEDICINES MAY INTERACT with Gynazole-1 Cream. However, no specific interactions with Gynazole-1 Cream are known at this time.

Ask your health care provider if Gynazole-1 Cream 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 Gynazole-1 Cream:

Use Gynazole-1 Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Gynazole-1 Cream is for vaginal use only. Do not use in the eyes or take by mouth. Wash your hands before and after using Gynazole-1 Cream. Insert 1 applicator-full of cream into the vagina. Throw the applicator away after using it. Only one dose of Gynazole-1 Cream is required. If you forget to use Gynazole-1 Cream, use it as soon as you remember.

Ask your health care provider any questions you may have about how to use Gynazole-1 Cream.

Important safety information: If your symptoms do not get better within a few days or if they get worse, check with your doctor. If your infection clears up and occurs again in a few weeks, see your doctor. Recurrent vaginal infections, especially those that are difficult to cure, may be an early sign of HIV infection in women who are considered at risk for HIV infection. Gynazole-1 Cream may be used during your period. Use a sanitary pad rather than a tampon to prevent staining of clothing. Gynazole-1 Cream contains mineral oil, which may weaken latex or rubber products such as condoms and diaphragms. Do not use condoms or diaphragms within 72 hours of using Gynazole-1 Cream. Gynazole-1 Cream should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Gynazole-1 Cream while you are pregnant. It is not known if Gynazole-1 Cream is found in breast milk. If you are or will be breast-feeding while you use Gynazole-1 Cream, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Gynazole-1 Cream:

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:

Burning, itching, soreness, or swelling in or around the vagina not present before using Gynazole-1 Cream.

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); pain or cramping in the stomach or pelvic area.

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: Gynazole-1 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. Gynazole-1 Cream may be harmful if swallowed.

Proper storage of Gynazole-1 Cream:

Store Gynazole-1 Cream at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Keep Gynazole-1 Cream out of the reach of children and away from pets.

General information: If you have any questions about Gynazole-1 Cream, please talk with your doctor, pharmacist, or other health care provider. Gynazole-1 Cream 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 Gynazole-1 Cream. 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 Gynazole-1 resources Gynazole-1 Side Effects (in more detail) Gynazole-1 Use in Pregnancy & Breastfeeding Gynazole-1 Support Group 2 Reviews for Gynazole-1 - Add your own review/rating Compare Gynazole-1 with other medications Vaginal Yeast Infection
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Quinocort Cream


1. Name Of The Medicinal Product QUINOCORT™ CREAM 2. Qualitative And Quantitative Composition

Potassium Hydroxyquinoline Sulphate BP

0.5%

Hydrocortisone BP

1.0%

3. Pharmaceutical Form

Quinocort Cream is a faintly yellow vanishing cream. It is intended for topical use only.

4. Clinical Particulars 4.1 Therapeutic Indications

The treatment of infected eczema, intertrigo and other steroid-responsive dermatoses where anti-infective cover is appropriate.

4.2 Posology And Method Of Administration

Route of administration: For topical use only.

Adults, children and the elderly

By gentle massage over all the affected area two to three times daily.

4.3 Contraindications

Patients with known sensitivity or intolerance to any of the ingredients.

4.4 Special Warnings And Precautions For Use

Contact with eyes and other mucosal surfaces should be avoided. Caution should be exercised when using this preparation in infants. Long term continuous topical therapy should be avoided in infants - adrenal suppression can occur even without occlusion.

4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction

Not applicable.

4.6 Pregnancy And Lactation

In pregnant animals administration of corticosteroids can cause abnormalities of foetal development. The relevance of this finding in human beings has not been established. However, topical steroids should not be used extensively in pregnancy i.e. in large amounts for long periods.

4.7 Effects On Ability To Drive And Use Machines

Not applicable.

4.8 Undesirable Effects

Not applicable.

4.9 Overdose

Not applicable.

5. Pharmacological Properties

Hydrocortisone provides anti-inflammatory action yet is the least potent topical corticosteroid available. Potassium hydroxyquinoline sulphate provides broad spectrum antibacterial and anticandidal activity. The combination facilitates treatment of steroid-responsive dermatoses where complication by infection with bacteria or yeasts is evident suspected, or a possibility.

6. Pharmaceutical Particulars 6.1 List Of Excipients

Lactic Acid BP, White Soft Paraffin BP, Edetic Acid BP, Sodium Acid Phosphate BP, Maize Starch BP, cetyl stearyl alcohol, sodium cetyl stearyl sulphate, PEG 40 castor oil, Chlorocresol BP, Purified Water BP.

6.2 Incompatibilities

Not applicable.

6.3 Shelf Life

Two years.

6.4 Special Precautions For Storage

Quinocort Cream should be stored in a cool, dry place avoiding extremes of temperature i.e. not less than 5°C and not more than 30°C.

6.5 Nature And Contents Of Container

Quinocort Cream is available in heat sealed low density polyethylene tubes with flush fitting cap containing 30 g of product. Each tube is cartoned and contains a patient information leaflet.

6.6 Special Precautions For Disposal And Other Handling

For topical use only.

8. Marketing Authorisation Number(S)

0291/0014.

10. Date Of Revision Of The Text

May 1995.

Legal category

POM.


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AmLactin AP Cream


Generic Name: Ammonium Lactate/Pramoxine (ah-MOE-nee-uhm LACK-tate/pra-MOX-een)
Brand Name: AmLactin AP
AmLactin AP Cream is used for:

Treating itching due to dry skin and other minor skin irritations.

AmLactin AP Cream is a combination moisturizer and local anesthetic. It works by moisturizing the skin and decreasing itching in the affected area.

Do NOT use AmLactin AP Cream if: you are allergic to any ingredient in AmLactin AP Cream

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

Before using AmLactin AP Cream:

Some medical conditions may interact with AmLactin AP Cream. 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 any kind of skin infection, open cuts, or scrapes if you have a parasitic, bacterial, fungal, or viral infection of the affected area

Some MEDICINES MAY INTERACT with AmLactin AP Cream. Because little, if any, of AmLactin AP Cream is absorbed into the blood, the risk of it interacting with another medicine is low.

Ask your health care provider if AmLactin AP Cream 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 AmLactin AP Cream:

Use AmLactin AP Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

AmLactin AP Cream is for use on the skin only. If you miss a dose of AmLactin AP Cream and you are using it regularly, use it as soon as possible. If several hours have passed or if it is nearing time for the next dose, do not double the dose to catch up, unless advised by your health care provider. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use AmLactin AP Cream.

Important safety information: If your symptoms do not get better within 7 days or if they get worse, check with your doctor. Avoid getting AmLactin AP Cream in your eyes, nose, or mouth. If you get AmLactin AP Cream in your eyes, immediately flush them with cool tap water. AmLactin AP Cream may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to AmLactin AP Cream. Use a sunscreen or wear protective clothing if you must be outside for more than a short time. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using AmLactin AP Cream while you are pregnant. It is not known if AmLactin AP Cream is found in breast milk after topical use. If you are or will be breast-feeding while you use AmLactin AP Cream, check with your doctor. Discuss any possible risks to your baby. Possible side effects of AmLactin AP Cream:

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:

Dry skin; itching.

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).

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: AmLactin AP 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 increased thirst or urination; muscle weakness; unusual weight gain, especially in the face. AmLactin AP Cream may be harmful if swallowed.

Proper storage of AmLactin AP Cream:

Store AmLactin AP Cream 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 AmLactin AP Cream out of the reach of children and away from pets.

General information: If you have any questions about AmLactin AP Cream, please talk with your doctor, pharmacist, or other health care provider. AmLactin AP Cream 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.

This information is a summary only. It does not contain all information about AmLactin AP Cream. 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 AmLactin AP resources AmLactin AP Side Effects (in more detail)AmLactin AP Use in Pregnancy & BreastfeedingAmLactin AP Support Group0 Reviews for AmLactin AP - Add your own review/rating Compare AmLactin AP with other medications Dry Skin
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Povidone/Iodine Cream


Pronunciation: POE-vi-done/EYE-oh-dine
Generic Name: Povidone/Iodine
Brand Name: Examples include Betadine and Pharmadine
Povidone/Iodine Cream is used for:

Treating minor wounds and infections, as well as killing bacteria.

Povidone/Iodine Cream is an antiseptic combination. It works by killing sensitive bacteria.

Do NOT use Povidone/Iodine Cream if: you are allergic to any ingredient in Povidone/Iodine Cream

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

Before using Povidone/Iodine Cream:

Some medical conditions may interact with Povidone/Iodine Cream. 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 serious burns or deep puncture wounds

Some MEDICINES MAY INTERACT with Povidone/Iodine Cream. However, no specific interactions are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Povidone/Iodine Cream 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 Povidone/Iodine Cream:

Use Povidone/Iodine Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Clean the affected area. Apply a small amount of Povidone/Iodine Cream to the affected area. The area may be left uncovered, or you may cover it with a sterile bandage. If you miss a dose of Povidone/Iodine Cream, use 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 use 2 doses at once.

Ask your health care provider any questions you may have about how to use Povidone/Iodine Cream.

Important safety information: If you have had a severe allergic reaction to Povidone/Iodine Cream or a medicine that contains iodine, contact your doctor or pharmacist immediately. A severe allergic reaction includes a severe rash, hives, difficulty breathing, or dizziness. If you have questions about whether you are allergic to Povidone/Iodine Cream or if a certain medicine contains iodine, contact your doctor or pharmacist. If you experience a skin rash, hives, or itching, or any other unusual reaction after using this product, discontinue use and contact your doctor as soon as possible. Povidone/Iodine Cream is for external use only. Do not get Povidone/Iodine Cream in your eyes. Do not use Povidone/Iodine Cream over large areas of the body or for more than 1 week unless advised to do so by your doctor. Contact your doctor before using Povidone/Iodine Cream on serious burns, deep wounds, or puncture wounds. PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Povidone/Iodine Cream, discuss with your doctor the benefits and risks of using Povidone/Iodine Cream during pregnancy. It is unknown if Povidone/Iodine Cream is excreted in breast milk. If you are or will be breast-feeding while you are using Povidone/Iodine Cream, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Povidone/Iodine Cream:

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:

Skin irritation.

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).

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.

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.

Proper storage of Povidone/Iodine Cream:

Store Povidone/Iodine Cream at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Povidone/Iodine Cream out of the reach of children and away from pets.

General information: If you have any questions about Povidone/Iodine Cream, please talk with your doctor, pharmacist, or other health care provider. Povidone/Iodine Cream 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 Povidone/Iodine Cream. 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 Povidone/Iodine resources Povidone/Iodine Use in Pregnancy & Breastfeeding Povidone/Iodine Support Group 0 Reviews · Be the first to review/rate this drug
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AmLactin Cream


Pronunciation: LACK-tick ASS-id
Generic Name: Lactic Acid
Brand Name: Examples include AmLactin and Lac-Hydrin
AmLactin Cream is used for:

Treating mild to severe forms of dry, scaly skin.

AmLactin Cream is a humectant. Exactly how it works is unknown but it increases the amount of water in the skin, making it softer and more pliable.

Do NOT use AmLactin Cream if: you are allergic to any ingredient in AmLactin Cream

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

Before using AmLactin Cream:

Some medical conditions may interact with AmLactin Cream. 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

Some MEDICINES MAY INTERACT with AmLactin Cream. Because little, if any, of AmLactin Cream is absorbed into the blood, the risk of it interacting with another medicine is low.

This may not be a complete list of all interactions that may occur. Ask your health care provider if AmLactin Cream 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 AmLactin Cream:

Use AmLactin Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Apply AmLactin Cream to the affected area and rub in thoroughly twice daily or as directed by your health care provider. Wash your hands immediately after using AmLactin Cream, unless your hands are part of the treated area. If you miss a dose of AmLactin Cream, use 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 use 2 doses at once.

Ask your health care provider any questions you may have about how to use AmLactin Cream.

Important safety information: AmLactin Cream may cause stinging or burning when applied to cracked or scraped skin (eg, after shaving). AmLactin Cream is for external use only. Avoid contact with the eyes, lips, or mucous membranes. AmLactin Cream may be harmful if swallowed. If you or someone you know may have taken AmLactin Cream by mouth, contact your local poison control center or emergency room immediately. Overuse of topical products may worsen your condition. AmLactin Cream may cause increased sensitivity to the sun. Avoid exposure to the sun, sunlamps, or tanning booths until you know how you react to AmLactin Cream. Use a sunscreen or protective clothing if you must be outside for a prolonged period. PREGNANCY and BREAST-FEEDING: If you plan on becoming pregnant, discuss with your doctor the benefits and risks of using AmLactin Cream during pregnancy. It is unknown if AmLactin Cream is excreted in breast milk. If you are or will be breast-feeding while you are using AmLactin Cream, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of AmLactin Cream:

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:

Burning; dry skin; flushing; irritation; itching; rash; stinging.

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); worsening of condition.

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: AmLactin 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. AmLactin Cream may be harmful if swallowed.

Proper storage of AmLactin Cream:

Store at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Keep AmLactin Cream out of the reach of children and away from pets.

General information: If you have any questions about AmLactin Cream, please talk with your doctor, pharmacist, or other health care provider. AmLactin Cream 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 AmLactin Cream. 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 AmLactin resources AmLactin Side Effects (in more detail) AmLactin Use in Pregnancy & Breastfeeding AmLactin Support Group 0 Reviews for AmLactin - Add your own review/rating Compare AmLactin with other medications Dry Skin Pityriasis rubra pilaris
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Ammonium Lactate/Pramoxine Cream


Generic Name: Ammonium Lactate/Pramoxine (ah-MOE-nee-uhm LACK-tate/pra-MOX-een)
Brand Name: AmLactin AP
Ammonium Lactate/Pramoxine Cream is used for:

Treating itching due to dry skin and other minor skin irritations.

Ammonium Lactate/Pramoxine Cream is a combination moisturizer and local anesthetic. It works by moisturizing the skin and decreasing itching in the affected area.

Do NOT use Ammonium Lactate/Pramoxine Cream if: you are allergic to any ingredient in Ammonium Lactate/Pramoxine Cream

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

Before using Ammonium Lactate/Pramoxine Cream:

Some medical conditions may interact with Ammonium Lactate/Pramoxine Cream. 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 any kind of skin infection, open cuts, or scrapes if you have a parasitic, bacterial, fungal, or viral infection of the affected area

Some MEDICINES MAY INTERACT with Ammonium Lactate/Pramoxine Cream. Because little, if any, of Ammonium Lactate/Pramoxine Cream is absorbed into the blood, the risk of it interacting with another medicine is low.

Ask your health care provider if Ammonium Lactate/Pramoxine Cream 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 Ammonium Lactate/Pramoxine Cream:

Use Ammonium Lactate/Pramoxine Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ammonium Lactate/Pramoxine Cream is for use on the skin only. If you miss a dose of Ammonium Lactate/Pramoxine Cream and you are using it regularly, use it as soon as possible. If several hours have passed or if it is nearing time for the next dose, do not double the dose to catch up, unless advised by your health care provider. Do not use 2 doses at once.

Ask your health care provider any questions you may have about how to use Ammonium Lactate/Pramoxine Cream.

Important safety information: If your symptoms do not get better within 7 days or if they get worse, check with your doctor. Avoid getting Ammonium Lactate/Pramoxine Cream in your eyes, nose, or mouth. If you get Ammonium Lactate/Pramoxine Cream in your eyes, immediately flush them with cool tap water. Ammonium Lactate/Pramoxine Cream may cause you to become sunburned more easily. Avoid the sun, sunlamps, or tanning booths until you know how you react to Ammonium Lactate/Pramoxine Cream. Use a sunscreen or wear protective clothing if you must be outside for more than a short time. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Ammonium Lactate/Pramoxine Cream while you are pregnant. It is not known if Ammonium Lactate/Pramoxine Cream is found in breast milk after topical use. If you are or will be breast-feeding while you use Ammonium Lactate/Pramoxine Cream, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Ammonium Lactate/Pramoxine Cream:

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:

Dry skin; itching.

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).

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: Ammonium Lactate/Pramoxine 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 increased thirst or urination; muscle weakness; unusual weight gain, especially in the face. Ammonium Lactate/Pramoxine Cream may be harmful if swallowed.

Proper storage of Ammonium Lactate/Pramoxine Cream:

Store Ammonium Lactate/Pramoxine Cream 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 Ammonium Lactate/Pramoxine Cream out of the reach of children and away from pets.

General information: If you have any questions about Ammonium Lactate/Pramoxine Cream, please talk with your doctor, pharmacist, or other health care provider. Ammonium Lactate/Pramoxine Cream 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.

This information is a summary only. It does not contain all information about Ammonium Lactate/Pramoxine Cream. 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 Ammonium Lactate/Pramoxine resources Ammonium Lactate/Pramoxine Side Effects (in more detail) Ammonium Lactate/Pramoxine Use in Pregnancy & Breastfeeding Ammonium Lactate/Pramoxine Support Group 0 Reviews for Ammonium Lactate/Pramoxine - Add your own review/rating Compare Ammonium Lactate/Pramoxine with other medications Dry Skin
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Sodium Fluoride Cream


Pronunciation: SO-dee-um FLOR-ide
Generic Name: Sodium Fluoride
Brand Name: Examples include Phos-Flur and PreviDent
Sodium Fluoride Cream is used for:

Preventing dental caries.

Sodium Fluoride Cream is a fluoride-containing toothpaste. It works by strengthening the teeth and decreasing the effects of acid and bacteria on the teeth.

Do NOT use Sodium Fluoride Cream if: you are allergic to any ingredient in Sodium Fluoride Cream you have trouble swallowing

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

Before using Sodium Fluoride Cream:

Some medical conditions may interact with Sodium Fluoride Cream. 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

Some MEDICINES MAY INTERACT with Sodium Fluoride Cream. However, no specific interactions with Sodium Fluoride Cream are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Sodium Fluoride Cream 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 Sodium Fluoride Cream:

Use Sodium Fluoride Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Brush your teeth with a small amount of Sodium Fluoride Cream. Swish it around your mouth for about 1 minute and then spit it out. Do not swallow it. Do not eat, drink, or rinse your mouth for 30 minutes after using Sodium Fluoride Cream. If you miss a dose of Sodium Fluoride Cream, 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 Sodium Fluoride Cream.

Important safety information: Do not exceed the dose recommended by your doctor or dentist. Notify your dentist if your teeth become spotted or stained. Caution is advised when using Sodium Fluoride Cream in CHILDREN; they may be more sensitive to its effects PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Sodium Fluoride Cream, discuss with your doctor the benefits and risks of using Sodium Fluoride Cream during pregnancy. It is not known if Sodium Fluoride Cream is found in breast milk. If you are or will be breast-feeding while you are using Sodium Fluoride Cream, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Sodium Fluoride Cream:

All medicines may cause side effects, but many people have no, or minor, side effects. When used in small doses, no COMMON side effects have been reported with Sodium Fluoride Cream. 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).

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.

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 diarrhea; extreme thirst; increased drooling; muscle weakness; nausea; paleness of the skin; seizures; shallow, rapid breathing; shaking; stomach pain; vomiting; weak or fast heartbeat.

Proper storage of Sodium Fluoride Cream:

Store Sodium Fluoride Cream at room temperature, between 68 and 77 degrees F (20 and 25 degrees C), in a tightly closed container. Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Sodium Fluoride Cream out of the reach of children and away from pets.

General information: If you have any questions about Sodium Fluoride Cream, please talk with your doctor, pharmacist, or other health care provider. Sodium Fluoride Cream 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 Sodium Fluoride Cream. 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 Sodium Fluoride resources Sodium Fluoride Use in Pregnancy & Breastfeeding Sodium Fluoride Support Group 3 Reviews for Sodium Fluoride - Add your own review/rating Compare Sodium Fluoride with other medications Prevention of Dental Caries
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Exelderm Cream


Pronunciation: sul-KON-a-zole
Generic Name: Sulconazole
Brand Name: Exelderm
Exelderm Cream is used for:

Treating fungal infections, such as jock itch, athlete's foot, ringworm, and tinea versicolor (a fungal infection affecting the skin of the upper arms, chest, back, and sometimes the neck and face).

Exelderm Cream is an antifungal. It works by blocking the growth of fungi.

Do NOT use Exelderm Cream if: you are allergic to any ingredient in Exelderm Cream

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

Before using Exelderm Cream:

Some medical conditions may interact with Exelderm Cream. 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

Some MEDICINES MAY INTERACT with Exelderm Cream. Because little, if any, of Exelderm Cream is absorbed into the blood, the risk of it interacting with another medicine is low.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Exelderm Cream 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 Exelderm Cream:

Use Exelderm Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

To clear up your infection completely, continue using Exelderm Cream for the full course of treatment. Exelderm Cream is for external use only. Clean the affected area with soap and water and dry thoroughly. Apply enough medicine to cover the affected area. Rub in gently. Do not cover unless directed otherwise by your doctor. Wash your hands immediately after using Exelderm Cream, unless your hands are part of the treated area. If you miss a dose of Exelderm Cream, use 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.

Ask your health care provider any questions you may have about how to use Exelderm Cream.

Important safety information: Exelderm Cream is for external use only. Do not get Exelderm Cream in your eyes. Exelderm Cream may be harmful if swallowed. If you may have taken Exelderm Cream by mouth, contact your local poison control center or emergency room immediately. Overuse of topical products may worsen your condition. If your condition does not improve within 4 to 6 weeks or if it gets worse, check with your doctor. Use Exelderm Cream with caution in the ELDERLY because they may be more sensitive to its effects. Use Exelderm Cream with extreme caution in CHILDREN. Safety and effectiveness have not been confirmed. PREGNANCY and BREAST-FEEDING: If you become pregnant, discuss with your doctor the benefits and risks of using Exelderm Cream during pregnancy. It is unknown if Exelderm Cream is excreted in breast milk. If you are or will be breast-feeding while you are using Exelderm Cream, check with your doctor or pharmacist to discuss the risks to your baby. Possible side effects of Exelderm Cream:

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:

Burning; itching; redness; stinging.

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: Exelderm 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.

Proper storage of Exelderm Cream:

Store Exelderm Cream at room temperature. Avoid temperatures above 104 degrees F (40 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Exelderm Cream out of the reach of children and away from pets.

General information: If you have any questions about Exelderm Cream, please talk with your doctor, pharmacist, or other health care provider. Exelderm Cream 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 Exelderm Cream. 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 Exelderm resources Exelderm Side Effects (in more detail) Exelderm Use in Pregnancy & Breastfeeding Exelderm Support Group 0 Reviews for Exelderm - Add your own review/rating Compare Exelderm with other medications Impetigo Tinea Corporis Tinea Cruris Tinea Pedis Tinea Versicolor
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Mentax Cream


Pronunciation: byoo-TEN-a-feen
Generic Name: Butenafine
Brand Name: Mentax
Mentax Cream is used for:

Treating certain fungal infections of the skin. It may also be used to treat other conditions as determined by your doctor, which may not be listed in the professional package insert.

Mentax Cream is a topical antifungal. It works by killing sensitive fungi by interfering with the formation of the fungal cell membrane and weakening it.

Do NOT use Mentax Cream if: you are allergic to any ingredient in Mentax Cream

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

Before using Mentax Cream:

Some medical conditions may interact with Mentax Cream. 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

Some MEDICINES MAY INTERACT with Mentax Cream. However, no specific interactions with Mentax Cream are known at this time.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Mentax Cream 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 Mentax Cream:

Use Mentax Cream as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Mentax Cream works best if it is used at the same time(s) each day. Wash and completely dry the affected area. Gently rub the medicine in until it is evenly distributed. Use enough cream to cover the affected areas and the healthy skin close to the affected areas. Wash your hands immediately after using Mentax Cream. Do not cover the area with bandages or other dressings unless directed by your health care provider. Continue to use Mentax Cream for the full treatment time recommended by your health care provider, even though symptoms have gotten better. If you miss a dose of Mentax Cream, use 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 use 2 doses at once.

Ask your health care provider any questions you may have about how to use Mentax Cream.

Important safety information: Do not use Mentax Cream for other skin conditions at a later time. Mentax Cream is for external use only. Avoid contact with nose, mouth, and eyes. If you get Mentax Cream in your eyes, immediately rinse out with cool tap water. Mentax Cream is not for use in CHILDREN younger than 12 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 Mentax Cream during pregnancy. It is unknown if Mentax Cream is excreted in breast milk. If you are or will be breast-feeding, check with your doctor to discuss the benefits and risks to your baby. Possible side effects of Mentax Cream:

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:

Burning; inflammation; irritation; itching; redness; stinging.

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: Mentax 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. Mentax Cream may be harmful if swallowed.

Proper storage of Mentax Cream:

Store Mentax Cream at room temperature between 59 and 86 degrees F (15 and 30 degrees C) in a tightly-closed container, away from heat, moisture, and light. Do not store in the bathroom. Keep Mentax Cream out of the reach of children and away from pets.

General information: If you have any questions about Mentax Cream, please talk with your doctor, pharmacist, or other health care provider. Mentax Cream 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 Mentax Cream. 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 Mentax resources Mentax Side Effects (in more detail) Mentax Use in Pregnancy & Breastfeeding Mentax Support Group 0 Reviews for Mentax - Add your own review/rating Compare Mentax with other medications Tinea Corporis Tinea Cruris Tinea Pedis
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