Xurea

Manufacturer
NATIONAL BIO GREEN SCIENCES LIMITED LIABILITY COMPANY
Effective date
2019-10-11
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 20:29:56

Label at a glance#

ProductXurea
Active ingredientUREA
Label structure15 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 prurient 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 dev...

Dosage and administration

Apply Xurea Cream to affected skin two to three times per day as needed or as directed by a physician. Rub in until completely absorbed. Apply to diseased or damaged nail tissue two to three times per day or as directed by a physician. Best applied to affected areas immediately after showering and just before bedtime.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Xurea (Urea 39% Cream) Rx only
For Topical Dermatological Use Only
Rx Only - Caution: Federal Law restricts this product to sale by, or on the order of a licensed healthcare practitioner.

Xurea Description

DESCRIPTION SECTION

Xurea Cream is a potent keratolytic emollient which is a gentle, yet potent, tissue softener for skin and/or nails.
Each gram of Xurea Cream contains:
ACTIVE: 39% Urea in a cream base of:
INACTIVES: Aqua (Deionized Water), Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Propylene Glycol, Dimethicone, Melaleuca Alternifolia (Tea Tree) Oil, Helianthus Annuus (Sunflower) Oil, Chamomilla Recutita (Chamomile) Extract, Carbomer, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin.

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

image descriptionimage description

Xurea - 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. 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

PHARMACOKINETICS SECTION

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

INDICATIONS AND USES

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 prurient 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

CONTRAINDICATIONS SECTION

Xurea Cream is contraindicated in patients with known hypersensitivity to any of the listed ingredients.

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes, lips or mucous membranes. Do not use on areas of broken skin.

Precautions

PRECAUTIONS SECTION

Stop use and ask a doctor if redness or irritation develops. After applying this medication, wash hands and unaffected areas thoroughly. If swallowed, get medical help or contact Poison Control Center right away. KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

PREGNANCY

PREGNANCY SECTION

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 reproduction studies are not always predictive of human response, Xurea Cream should be given to a pregnant woman only if clearly needed.

NURSING MOTHERS

NURSING MOTHERS SECTION

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 Xurea Cream is administered to a nursing woman.

Adverse Reactions

ADVERSE REACTIONS SECTION

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

Xurea - Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Apply Xurea Cream to affected skin two to three times per day as needed or as directed by a physician. Rub in until completely absorbed. Apply to diseased or damaged nail tissue two to three times per day or as directed by a physician. Best applied to affected areas immediately after showering and just before bedtime.

How is Xurea Supplied

HOW SUPPLIED SECTION

Xurea (39% Urea Cream) is supplied in:


8oz (227gm) Jar      NDC 72678-034-01

Store at 25°C (77°F); excursions permitted to 15°C - 30°C (59° - 86°F). Protect from freezing. [See USP Controlled Room Temperature.]

Manufactured for:
NATIONAL BIO GREEN SCIENCES LIMITED LIABILITY COMPANY
Branchburg, NJ 08876

Rx only

SPL UNCLASSIFIED SECTION

PRINCIPAL DISPLAY PANEL - 227 gm Jar Label

Rx only

NDC 72678-034-01

Xurea UREA 39% CREAM

Smooth - Spreadable - Moisturizing

Xurea’s high amount of urea exhibits intensive keratolyic and peeling effects. Thoroughly nourishes, helping to prevent cracks, and drying of your skin.

FOR TOPICAL USE ONLY

Net WT. 8OZ (227 gm)

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1093289urea 39 % Topical CreamPSN3
1093289urea 390 MG/ML Topical CreamSCD3
1093289urea 39 % Topical CreamSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72678-034-012021-01-29C16284748780-1ba0f9c33-3d9e-a910-e053-dadaa90a0b85Xurea

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72678-034-01Xurea227 g in 1 JARCREAM2273

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72678-034XUREA (UREA) CREAM [NATIONAL BIO GREEN SCIENCES LIMITED LIABILITY COMPANY]3Legacy NDC, 1 package rows20191012_bfbd3916-dfef-4192-a99e-ee9f97a3f532.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72678-034-01GM - Gram72678-034b1fdbc11-5c1d-45f9-941a-a995cec762cf12019-11-12

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72678-03472678-034-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5e3c2d89-edb8-48e9-aa89-9dab6bd0f957bfbd3916-dfef-4192-a99e-ee9f97a3f5322019-10-11Warnings, Adverse reactionsExact identifier
spl id: 5e3c2d89-edb8-48e9-aa89-9dab6bd0f957
spl set id: bfbd3916-dfef-4192-a99e-ee9f97a3f532

Reported adverse events (FAERS/openFDA)#

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