umecta cream
 

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ED Pills

ED Drugs
 

Umecta PD


urea
Dosage Form: topical emulsion
Umecta PD Description
Rx only
For topical use only
Not for ophthalmic use
Umecta is a keratolytic, emollient which is a gentle, yet potent, tissue softener for nails and skin
Each gram of Umecta PD bioadhesive emulsion and topical suspension contains40% urea, sodium hyaluronate 0.3%, BHT, butyrospermum parkii fruit oil, citric acid, dimethylacrylamide (and) acrylic acid (and) polystyrene ethyl methacrylate copolymer, disodium EDTA, glyceryl stearate, glycine soja sterol, helianthus annuus oil, hydroxypropylmethyl cellulose, purified water, sodium citrate, stearic acid.
Clinical Pharmacology
Urea gently dissolves the intercellular matrix which results in loosening the horny layer of skin and shedding scaly skin at regular intervals, thereby softening hyperkeratotic areas. Urea also hydrates and gently dissolves the intercellular matrix of the nail plate which can result in the softening and eventual debridement of the nail plate.
Pharmacokinetics

The mechanism of action of topically applied urea is not yet known.

Indications and Uses

For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent debris or eschar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis, keratoderma, corns, and calluses, as well as damaged, ingrown and devitalized nails.

Contraindications Known hypersensitivity to any of the listed ingredients. Warnings

For external use only. Avoid contact with eyes, lips or mucous membranes.


Precautions This medication is to be used as directed by a physician and should not be used to treat any condition other than that for which it was prescribed. If redness or irritation occurs, discontinue use.
Pregnancy Category C Animal reproduction studies have not been conducted with Umecta. It is also not known whether Umecta can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Umecta should be given to a pregnant woman only if clearly needed. Nursing Mothers

It is not known whether or not this drug is secreted in human milk. Because many drugs are secreted in human milk, caution should be exercised when Umecta is administered to a nursing woman.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

Adverse Reactions

Transient stinging, burning, itching, or irritation may occur and normally disappear on discontinuing the medication.

Dosage and Administration Apply Umecta emulsion/topical suspension or Umecta mousse to affected skin twice per day or as directed by a physician. Rub in until completely absorbed. How Supplied
Umecta PD™ (urea, 40% - sodium hyaluronate 0.3%) bioadhesive emulsion is available in a:7 oz. bottle NDC 68712-017-02
Store at controlled room temperature 15-30°C (59-86°F).

Manufactured for:

Innocutis Holdings LLC
Charleston, SC 29401
Toll Free: 1-800-499-4468
www.innocutis.com
www.umecta.com







Umecta PD  UREA
urea   emulsion Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 68712-017 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UREA (UREA) UREA 400 mg  in 1 g Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE   SHEA BUTTER   CITRIC ACID MONOHYDRATE   EDETATE DISODIUM   GLYCERYL MONOSTEARATE   SOYBEAN OIL   SUNFLOWER OIL   HYPROMELLOSES   WATER   SODIUM CITRATE   STEARIC ACID   HYALURONATE SODIUM   Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 68712-017-01 3 g In 1 PACKET None 2 68712-017-02 198.5 g In 1 BOTTLE None
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/01/2007
Labeler - Innocutis Holdings LLC (071501252) Establishment Name Address ID/FEI Operations Sonar Products 104283945 manufacture Revised: 12/2011Innocutis Holdings LLC More Umecta PD resources Umecta PD Side Effects (in more detail) Umecta PD Use in Pregnancy & Breastfeeding Umecta PD Support Group 0 Reviews for Umecta PD - Add your own review/rating Umecta PD Topical Suspension MedFacts Consumer Leaflet (Wolters Kluwer) Aqua Care Cream MedFacts Consumer Leaflet (Wolters Kluwer) Hydro 35 Foam MedFacts Consumer Leaflet (Wolters Kluwer) Kerafoam Foam MedFacts Consumer Leaflet (Wolters Kluwer) Keralac Cream MedFacts Consumer Leaflet (Wolters Kluwer) Keralac Nailstik Solution MedFacts Consumer Leaflet (Wolters Kluwer) Kerol MedFacts Consumer Leaflet (Wolters Kluwer) Ultra Mide Topical Advanced Consumer (Micromedex) - Includes Dosage Information Umecta Nail Film MedFacts Consumer Leaflet (Wolters Kluwer) Uramaxin Foam MedFacts Consumer Leaflet (Wolters Kluwer) Compare Umecta PD with other medications Dermatological Disorders Dry Skin Pityriasis rubra pilaris
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Aluvea


urea
Dosage Form: cream
Aluvea

(39% Urea Cream)

RX ONLY

Aluvea Description

Aluvea™ (urea) cream, 39% is a keratolytic emollient, which is a gentle, yet effective, tissue softener for skin.

Each gram of Aluvea Cream contains 39% Urea as the active ingredient, and the following inactive ingredients: dimethyl isosorbide, emulsifying wax NF, glycerin 99.7% USP, isopropyl myristate, purified water, sorbitol 70% Solution USP, tridecyl stearate and neopentyl glycol dicaprylate/dicaprate and tridecyl trimellitate.

CHEMICAL STRUCTURE

Urea is diamide of Carbonic acid with the following structure:

Aluvea - Clinical Pharmacology

Urea gently dissolves the intracellular matrix which results in loosening of the horny layer of the skin and shedding of scaly skin at regular intervals, thereby softening hyperkeratotic areas of the skin.

PHARMACOKINETICS

The exact mechanism of action of topically applied urea is not known.

INDICATION AND USAGE

Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, xerosis, ichthyosis, skin cracks and fissures, dermatitis, eczema, psoriasis, keratoses and calluses.

Contraindications

Known hypersensitivity to any of the listed ingredients

Warnings

For external use only. Avoid contact with eyes, lips or mucous membranes.

Precautions

Urea should be used as directed by a physician and should not be used to treat conditions other than those for which it was prescribed. If redness or irritation occurs, discontinue use.

Pregnancy Category C

Animal reproduction studies have not been conducted with Aluvea. It is also not known whether Aluvea can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Aluvea should be given to a pregnant woman only if clearly needed.

Nursing Mothers

It is not known whether Aluvea is excreted in human milk, therefore caution should be exercised when administering to a nursing mother.

Adverse Reactions

Transient stinging, burning, itching or irritation is possible and normally resolves upon discontinuing the medication.

DOSAGE AND ADMINISTRATIONS

Apply Aluvea to affected skin twice per day, or as directed by your physician. Rub in until completely absorbed.

KEEP THIS AND ALL OTHER MEDICATIONS OUT OF REACH OF CHILDREN How is Aluvea Supplied

Aluvea is supplied in an 8oz. bottle.

NDC 0259-1139-80

Store at room temperature 15°C -30°C (59°F-86°F).

Protect from freezing.

Manufactured for:
Merz Pharmaceuticals, LLC
Greensboro, NC 27410

5011457 12/10

PRINCIPAL DISPLAY PANEL - 227g Carton

NDC 0259-1139-80

Aluvea™
39% Urea Cream

WITH UNIQUE
CSP ™
VEHICLE
TECHNOLOGY

FOR EXTERNAL USE ONLY

8 oz. (227g)

Rx ONLY


Aluvea 
urea  cream Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0259-1139 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Urea (Urea) Urea 39 g  in 100 g Inactive Ingredients Ingredient Name Strength Dimethyl isosorbide   Glycerin   Isopropyl Myristate   Sorbitol   Tridecyl Stearate   Neopentyl Glycol Dicaprate   Tridecyl Trimellitate   Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 0259-1139-80 1 BOTTLE In 1 CARTON contains a BOTTLE 1 227 g In 1 BOTTLE This package is contained within the CARTON (0259-1139-80)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 04/15/2011
Labeler - Merz Pharmaceuticals, LLC (126209282) Establishment Name Address ID/FEI Operations Crown Laboratories, Inc. 079035945 MANUFACTURE Revised: 04/2011Merz Pharmaceuticals, LLC More Aluvea resources Aluvea Side Effects (in more detail) Aluvea Use in Pregnancy & Breastfeeding Aluvea Support Group 0 Reviews for Aluvea - Add your own review/rating Aqua Care Cream MedFacts Consumer Leaflet (Wolters Kluwer) Hydro 35 Foam MedFacts Consumer Leaflet (Wolters Kluwer) Kerafoam Foam MedFacts Consumer Leaflet (Wolters Kluwer) Keralac Cream MedFacts Consumer Leaflet (Wolters Kluwer) Keralac Nailstik Solution MedFacts Consumer Leaflet (Wolters Kluwer) Kerol MedFacts Consumer Leaflet (Wolters Kluwer) Ultra Mide Topical Advanced Consumer (Micromedex) - Includes Dosage Information Umecta Nail Film MedFacts Consumer Leaflet (Wolters Kluwer) Umecta PD Topical Suspension MedFacts Consumer Leaflet (Wolters Kluwer) Uramaxin Foam MedFacts Consumer Leaflet (Wolters Kluwer) Compare Aluvea with other medications Dermatological Disorders Dry Skin Pityriasis rubra pilaris
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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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Kerol


Pronunciation: LAK-tik/SAL-i-SIL-ik/ue-REE-a
Generic Name: Lactic Acid/Salicylic Acid/Urea
Brand Name: Kerol
Kerol is used for:

Treating dry, rough, scaly skin caused by certain conditions (eg, dermatitis, psoriasis, eczema, corns, calluses). It may also be used for other conditions as determined by your doctor.

Kerol is a keratolytic. It works by helping to loosen and shed hard, scaly skin.

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

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

Before using Kerol:

Some medical conditions may interact with Kerol. 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 the affected area is damaged or severely irritated

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

Ask your health care provider if Kerol 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 Kerol:

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

Wash your hands immediately before and after using Kerol unless your hands are part of the treated area. Apply Kerol to the affected skin as directed by your doctor. Rub in gently until the medicine is completely absorbed. If you miss a dose of Kerol and you are using it regularly, 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 Kerol.

Important safety information: Kerol is for external use only. Do not get it in your eyes, nose, mouth, or on your lips. If you get it in any of these areas, rinse right away with cool water. Do not use more than the recommended dose or use for longer than prescribed without checking with your doctor. Do not use Kerol for other skin conditions at a later time. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Kerol while you are pregnant. It is not known if Kerol is found in breast milk. If you are or will be breast-feeding while you use Kerol, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Kerol:

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:

Mild, temporary burning, itching, irritation, or stinging.

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); redness; severe or persistent burning or irritation.

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: Kerol 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 Kerol:

Store Kerol at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not freeze. Store away from heat and direct sunlight. Keep Kerol out of the reach of children and away from pets.

General information: If you have any questions about Kerol, please talk with your doctor, pharmacist, or other health care provider. Kerol 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 Kerol. 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 Kerol resources Kerol Side Effects (in more detail) Kerol Use in Pregnancy & Breastfeeding Kerol Support Group 0 Reviews for Kerol - Add your own review/rating Aluvea Prescribing Information (FDA) Kerafoam Prescribing Information (FDA) Kerafoam 42 Prescribing Information (FDA) Kerol AD Prescribing Information (FDA) Latrix Prescribing Information (FDA) Remeven Prescribing Information (FDA) Ultra Mide Topical Advanced Consumer (Micromedex) - Includes Dosage Information Umecta Mousse Prescribing Information (FDA) Umecta Nail Film Prescribing Information (FDA) Umecta PD Prescribing Information (FDA) Urea Nail Gel Prescribing Information (FDA) Urealac Prescribing Information (FDA) X-Viate Prescribing Information (FDA) Compare Kerol with other medications Dermatological Disorders Dry Skin Pityriasis rubra pilaris
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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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Urea Cloths


Pronunciation: ue-REE-a
Generic Name: Urea
Brand Name: Kerol Redi Cloths
Urea Cloths are used for:

Treating dry, rough, scaly skin caused by certain conditions (eg, dermatitis, psoriasis, eczema, corns, calluses). It may also be used for certain other skin conditions as determined by your doctor.

Urea Cloths are a debriding agent. It works by helping the breakdown of dead skin, which helps to loosen and shed hard and scaly skin. It also softens and moisturizes the skin.

Do NOT use Urea Cloths if: you are allergic to any ingredient in Urea Cloths

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

Before using Urea Cloths:

Some medical conditions may interact with Urea Cloths. 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 the affected area is broken or severely irritated

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

Ask your health care provider if Urea Cloths 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 Urea Cloths:

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

Wash your hands immediately before and after using Urea Cloths unless your hands are part of the treated area. Gently apply Urea Cloths to the affected skin as directed by your doctor. If you miss a dose of Urea Cloths and you are using it regularly, 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 Urea Cloths.

Important safety information: Urea Cloths are for external use only. Do not get it in your eyes, nose, mouth, or on your lips. If you get Urea Cloths in your eyes, rinse them right away with cool water. Do not apply to broken or severely irritated skin. Do not use more than the recommended dose or use for longer than prescribed without checking with your doctor. Do not use Urea Cloths for other skin conditions at a later time. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Urea Cloths while you are pregnant. It is not known if Urea Cloths are found in breast milk. If you are or will be breast-feeding while you use Urea Cloths, check with your doctor. Discuss any possible risks to your baby. Possible side effects of Urea Cloths:

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:

Mild, temporary burning, itching, irritation, or stinging.

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); redness; severe or persistent burning or irritation.

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 Urea Cloths:

Store Urea Cloths at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not freeze. Store away from heat, moisture, and light. Keep Urea Cloths out of the reach of children and away from pets.

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

This information is a summary only. It does not contain all information about Urea Cloths. 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 Urea resources Urea Use in Pregnancy & Breastfeeding Urea Support Group 9 Reviews for Urea - Add your own review/rating Aluvea Prescribing Information (FDA) Kerafoam Prescribing Information (FDA) Kerafoam 42 Prescribing Information (FDA) Kerol AD Prescribing Information (FDA) Latrix Prescribing Information (FDA) Remeven Prescribing Information (FDA) Ultra Mide Topical Advanced Consumer (Micromedex) - Includes Dosage Information Umecta Mousse Prescribing Information (FDA) Umecta Nail Film Prescribing Information (FDA) Umecta PD Prescribing Information (FDA) Urea Nail Gel Prescribing Information (FDA) Urealac Prescribing Information (FDA) X-Viate Prescribing Information (FDA) Compare Urea with other medications Dermatological Disorders Dry Skin Pityriasis rubra pilaris
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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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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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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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Kerafoam


urea
Dosage Form: aerosol, foam
Kerafoam
For softening, smoothing and removing rough scaling hyperkeratotic skin DESCRIPTION:

Kerafoam® Emollient Foam is a keratolytic emollient foam which is a tissue softener for skin and/or nails. Kerafoam Emollient Foam contains 30% urea USP in an aqueous based emollient foam vehicle. Each gram of Kerafoam Emollient Foam contains 30% urea USP, ammonium lactate, cetyl alcohol NF, emulsifying wax NF, methylparaben NF, propylene glycol USP, propylparaben NF, purified water USP, steareth-10. Also contains: Propellant HFA-134a (1,1,1,2-tetrafluoroethane).
Urea USP is a diamide of carbonic acid with the following chemical structure:

Kerafoam - Clinical Pharmacology

Urea gently lyses/dissolves the intercellular matrix of surface skin cells loosening and allowing a shedding of rough, thickened and scaly hyperkeratotic skin. Urea also moisturizes and softens skin.

INDICATIONS

For softening, smoothing and removing rough scaling hyperkeratotic skin in conditions such as xerosis, ichthyosis, skin cracks and fissures, dermatitis, eczema, psoriasis, keratoses and calluses.

Contraindications

Known hypersensitivity to any of the listed ingredients. Discontinue use if hypersensitivity is observed.

Warnings

FOR EXTERNAL USE ONLY. Avoid contact with eyes, lips or mucous membranes. Keep out of the reach of children. Contents under pressure. Do not puncture or incinerate container. Do not expose to temperatures above 120?F (49?C).

Precautions Information for patients:

This medication is to be used as directed by a physician and should not be used to treat any condition other than that for which it was prescribed. If redness or irritation occurs, discontinue use.

Pregnancy

Pregnancy Category C. Animal reproduction studies have not been conducted with Kerafoam Emollient Foam. It is not known whether Kerafoam Emollient Foam can cause fetal harm when administered to a  pregnant woman or can affect reproduction capacity. Kerafoam Emollient Foam should be given to a pregnant woman only if clearly needed.

Nursing Mothers

It is not known whether or not this drug is secreted in human milk. Because many drugs are secreted in human milk, caution should be exercised when Kerafoam Emollient Foam is administered to a nursing woman.

Adverse Reactions

Transient stinging, burning, itching or irritation may occur and normally disappear on discontinuing the medication.

Kerafoam Dosage and Administration

Shake Vigorously, Tap Bottom of Can, and Prime Before Initial Use. Shake Vigorously and Tap Before Each Use.
To Prime: After shaking, gently tap bottom of can onto palm of other hand or a solid surface at least 3 times. Hold the can upright, direct away from the patient, and firmly depress the actuator for 1 to 3 seconds or until foam begins to dispense. (If foam does not dispense within 3 seconds: re-shake can, gently tap bottom of can onto a solid surface at least 3 times, and depress the actuator again until foam begins to dispense.)
Before Each Use: Shake vigorously and gently tap bottom of can onto palm of other hand or a solid surface at least 3 times.
During Use: Holding can upright, dispense Kerafoam into palm of hand and apply to affected area twice per day, or as directed by a physician. Rub in until completely absorbed. Wipe off any excess foam from actuator after use.

How is Kerafoam Supplied

Kerafoam Emollient Foam is supplied in a 60 g (NDC# 16781-157-60) aluminum can.

Store at room temperature: 59? - 77?F (15? - 25?C). Protect from freezing. Store upright.

Patent Pending

P/N 2604 Rev. 3

Manufactured For:

Onset Therapeutics
Cumberland, RI 02864

(888) 713-8154
www.onsettx.com

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - Kerafoam Outer Carton - 5g

NDC 16781-157-06
Rx Only
Kerafoam®
Emollient Foam
Urea (30%)
For softening, smoothing, and removing rough scaling hyperkeratotic skin
See prescribing information enclosed

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - Kerafoam Inner Label - 5g

NDC 16781-157-06
Rx Only
Professional Sample
Not for Sale
Net Weight 5g
Kerafoam®
Emollient Foam
Urea (30%)
Sample will not dispense entire contents.


Kerafoam 
urea  aerosol, foam Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 16781-157 Route of Administration TOPICAL DEA Schedule      Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UREA (UREA) UREA 30 g  in 100 g Inactive Ingredients Ingredient Name Strength AMMONIUM LACTATE   PROPYLENE GLYCOL   CETYL ALCOHOL   PROPYLPARABEN   METHYLPARABEN   WATER   Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains          Packaging # NDC Package Description Multilevel Packaging 1 16781-157-06 6 CAN In 1 BOX contains a CAN 1 5 g In 1 CAN This package is contained within the BOX (16781-157-06) 2 16781-157-11 6 CAN In 1 BOX contains a CAN 2 10 g In 1 CAN This package is contained within the BOX (16781-157-11) 3 16781-157-60 1 CAN In 1 BOX contains a CAN 3 60 g In 1 CAN This package is contained within the BOX (16781-157-60) 4 16781-157-96 1 CAN In 1 BOX contains a CAN 4 100 g In 1 CAN This package is contained within the BOX (16781-157-96)
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 12/01/2006 12/31/2011
Labeler - Onset Dermatologics LLC (793223707) Registrant - Onset Dermatologics LLC (964275155) Establishment Name Address ID/FEI Operations Onset Dermatologics LLC 793223707 Manufacture Revised: 11/2011Onset Dermatologics LLC More Kerafoam resources Kerafoam Side Effects (in more detail) Kerafoam Use in Pregnancy & Breastfeeding Kerafoam Support Group 1 Review for Kerafoam - Add your own review/rating Kerafoam Foam MedFacts Consumer Leaflet (Wolters Kluwer) Aqua Care Cream MedFacts Consumer Leaflet (Wolters Kluwer) Hydro 35 Foam MedFacts Consumer Leaflet (Wolters Kluwer) Keralac Cream MedFacts Consumer Leaflet (Wolters Kluwer) Keralac Nailstik Solution MedFacts Consumer Leaflet (Wolters Kluwer) Kerol MedFacts Consumer Leaflet (Wolters Kluwer) Ultra Mide Topical Advanced Consumer (Micromedex) - Includes Dosage Information Umecta Nail Film MedFacts Consumer Leaflet (Wolters Kluwer) Umecta PD Topical Suspension MedFacts Consumer Leaflet (Wolters Kluwer) Uramaxin Foam MedFacts Consumer Leaflet (Wolters Kluwer) Compare Kerafoam with other medications Dermatological Disorders Dry Skin Pityriasis rubra pilaris
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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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