Urea Cream 40 Percent

Manufacturer
Bryant Ranch Prepack
Effective date
2025-11-12
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
100
Source
full-release
Hydrated at
2026-05-31 22:05:08

Label at a glance#

ProductUrea Cream 40 Percent
Active ingredientUREA
Label structure12 sections

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 pilaris, keratosis palmaris, keratoderma, corns and calluses, as well...

Dosage and administration

Apply Urea 40% to affected skin twice per day, or as directed by your physician. Rub in until completely absorbed. Apply to diseased or damaged nail(s) twice per day, or as directed by a physician.

Label contents#

Full prescribing information#

Description

DESCRIPTION SECTION

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:

Carbomer, Cetearyl Alcohol, Glycerin, Glyceryl Stearate SE, Mineral Oil, Purified Water, White Petrolatum.

Urea is a diamide of carbonic acid with the following chemical structure:

structurestructure

Clinical Pharmacology

CLINICAL PHARMACOLOGY SECTION

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 of the skin.

Pharmacokinetics

PHARMACOKINETICS SECTION

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

Indications and Usage

INDICATIONS & USAGE SECTION

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

CONTRAINDICATIONS SECTION

Known hypersensitivity to any of the listed ingredients.

Warnings

WARNINGS SECTION

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

Precautions

PRECAUTIONS SECTION

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 and consult a physician.

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: It is not known whether or not this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Urea 40% is administered to a nursing woman.

Adverse Reactions

ADVERSE REACTIONS SECTION

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

To report SUSPECTED ADVERSE REACTIONS, contact Method Pharmaceuticals, LLC at

1-877-250-3427; or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Apply Urea 40% to affected skin twice per day, or as directed by your physician. Rub in until completely absorbed.

Apply to diseased or damaged nail(s) twice per day, or as directed by a physician.

How Supplied

HOW SUPPLIED SECTION

Urea 40% Cream

1 oz. (28.35 g): NDC: 71335-2868-1

Store 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.

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

SPL UNCLASSIFIED SECTION

Manufactured for:

Method Pharmaceuticals, LLC

Southlake, Texas 76092

Rev. 09/23

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Urea Cream 40% #28.35

Label
Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198342urea 40 % Topical CreamPSN100
198342urea 400 MG/ML Topical CreamSCD100
198342urea 40 % Topical CreamSY100

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codedailymed.nlm.nih.gov/dailymed/search.cfm?query=71335-2868-1lbl713352868.jpg
Data codeCode 1287133528681lbl713352868.jpg
Data codeData Matrix0100363629103317211444981724013110LOT42832lbl713352868.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-2868-1Urea Cream 40 Percent28.35 g in 1 BOTTLECREAM28.35100

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-2868-1GM - Gram71335-286828c8cd5d-8c0e-4da0-9ee6-978d94bdfd4612026-01-08
58657-489-01GM - Gram58657-48920d012e2-af13-46bf-81c1-76f9bacd263b12023-12-05
58657-489-03GM - Gram58657-489fd5edf21-bdc1-45a1-88a2-6d84004ec6c612023-12-05
58657-489-07GM - Gram58657-4894bb1dd3c-81cd-4327-8524-d6a51c335c4b12026-03-17

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71335-286871335-2868-1
58657-489

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Urea Cream 40 PercentUREAMethod Pharmaceuticals, LLC0920f780-b504-1fea-e063-6394a90ae5a92026-01-15Warnings, Adverse reactionsExact identifier
ndc (product): 58657-489
Urea Cream 40 PercentUREABryant Ranch Prepack59afcfbe-fe04-49c9-b1c5-28f2c4311c012025-11-12Warnings, Adverse reactionsExact identifier
ndc (package): 71335-2868-1
ndc (product): 71335-2868
ndc11 (package): 71335286801
spl id: 8e9975a5-a55e-4037-89b8-8aa5c691fead
spl set id: 59afcfbe-fe04-49c9-b1c5-28f2c4311c01

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.