Urea 40 Percent UREA BRYANT RANCH PREPACK FDA Approved INGREDIENTS: Each gram of Urea Cream 40% contains Urea 40% and the following inactive ingredients: Carbomer, Cetearyl Alcohol, Glycerin, Glyceryl Stearate SE, Mineral Oil, Purified Water, White Petrolatum.
Generic: UREA
Mfr: BRYANT RANCH PREPACK FDA Rx Only
FunFoxMeds box
Substance Urea
Route
TOPICAL
Package NDC

Drug Facts

Composition & Profile

Strengths
40 %
Treats Conditions
Indications This Product 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

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UNII
8W8T17847W
Packaging

HOW SUPPLIED: Urea Cream 40% This product is supplied in the following size: 7oz NDC 63629-9267-1 Repackaged/Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504; Urea Cream 40% Label

Package Descriptions
  • HOW SUPPLIED: Urea Cream 40% This product is supplied in the following size: 7oz NDC 63629-9267-1 Repackaged/Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504
  • Urea Cream 40% Label

Overview

INGREDIENTS: Each gram of Urea Cream 40% contains Urea 40% and the following inactive ingredients: Carbomer, Cetearyl Alcohol, Glycerin, Glyceryl Stearate SE, Mineral Oil, Purified Water, White Petrolatum.

Indications & Usage

INDICATIONS: This product 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.

Dosage & Administration

: Use as directed by your physician. See label booklet for full Prescribing Information.

Warnings & Precautions
WARNINGS: FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE. KEEP OUT OF REACH OF CHILDREN. Avoid contact with eyes, lips and mucous membranes. General: This product 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 and consult a physician. Information for Patients: Patients should discontinue the use of this product if the condition becomes worse or if a rash develops in the area being treated or elsewhere. Avoid contact with eyes, lips and mucous membranes. Carcinogenesis, Mutagenesis and Impairment of Fertility: Long-term animal studies for carcinogenic potential have not been performed on this product to date. Studies on reproduction and fertility also have not been performed. Pregnancy: Category C . Animal reproduction studies have not been conducted with this product. It is also not known whether this product can affect reproduction capacity or cause fetal harm when administered to a pregnant woman. This product should be used by a pregnant woman only if clearly needed or when potential benefits outweigh potential hazards to the fetus. Nursing Mothers: It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when this product is administered to a nursing woman.
Contraindications

: This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.

Adverse Reactions

Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product.


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