Label: UREA 40%- urea cream
- NDC Code(s): 82429-308-15, 82429-308-24, 82429-308-25
- Packager: Gabar Health Sciences Corp.
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated October 21, 2023
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- Official Label (Printer Friendly)
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DESCRIPTION
Rx Only
For external use only. Not for ophthalmic use.
Description
Urea 40% is a keratolytic emollient which is a gentle, yet potent, tissue softener for nails and/or skin. Each gram of Urea 40% contains 40% urea as an active ingredient, and the following inactive ingredients: Water, Propylene Glycol, Glyceryl Stearate, Mineral Oil, Cetyl Alcohol, Carbomer, Petrolatum, Xanthan Gum and Sodium Hydroxide.
Urea is a diamide of carbonic acid with the following chemical structure:
- Clinical Pharmacology
- Pharmacokinetics
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Indications and Usage
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 pilaris, keratosis palmaris, keratoderma, corns and calluses, as well as damaged, ingrown and devitalized nails.
- Contraindications
- Warnings
- Precautions
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PREGNANCY
PREGNANCY: Pregnancy Category B. Animal reproduction studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. Because animal reproductive studies are not always predictive of human response, Urea 40% should be given to a pregnant woman only if clearly needed.
- NURSING MOTHERS
- Adverse Reactions
- Dosage and Administration
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How Supplied
Urea 40% Cream 1 oz. (28.35 g): NDC 82429-308-15
Urea 40% Cream 3 oz. (85 g): NDC 82429-308-24
Urea 40% Cream 7 oz. (198.4 g): NDC 82429-308-25Store at room temperature 15°C - 30°C (59°F-86°F). Protect from freezing. Keep bottle tightly closed.
KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
Manufactured for and distributed by:
Gabar Health Sciences Corp.
Atlanta, GA 30354 - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
UREA 40%
urea creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:82429-308 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength UREA (UNII: 8W8T17847W) (UREA - UNII:8W8T17847W) UREA 40 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) MINERAL OIL (UNII: T5L8T28FGP) CETYL ALCOHOL (UNII: 936JST6JCN) CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC) PETROLATUM (UNII: 4T6H12BN9U) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM HYDROXIDE (UNII: 55X04QC32I) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82429-308-15 1 in 1 CARTON 08/01/2022 1 28 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:82429-308-24 1 in 1 CARTON 08/01/2022 2 85 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:82429-308-25 1 in 1 CARTON 08/01/2022 3 198 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2022 Labeler - Gabar Health Sciences Corp. (118401847) Registrant - Gabar Health Sciences Corp. (118401847)