FDA Label for Ure-k

View Indications, Usage & Precautions

Ure-k Product Label

The following document was submitted to the FDA by the labeler of this product Solutech Pharmaceuticals Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Other



Rx only

For external use only.
Not for ophthalmic use.


Ure-K 50% Description



URE-K 50% cream is a potent keratolytic emollient which is a gentle, yet potent, tissue softener for skin and/or nails.

Each gram of URE-K 50% cream contains:

ACTIVE: 50% Urea in a cream base of:

INACTIVES: Mineral Oil, Stearic Acid, Water, Glycerin, Polysorbate 20, Sepigel 305, Phenoxyethanol, Acrylate Copolymer and Vitamin E


Chemistry



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


Ure-K 50% - 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 Usage



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



URE-K 50% cream is contraindicated in patients with known hypersensitivity to any of the listed ingredients.


Warnings



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


Precautions



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


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, URE-K 50% cream 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 URE-K 50% cream is administered to a nursing woman.


Adverse Reactions



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


Ure-K 50% - Dosage And Administration



Apply URE-K 50% cream to affected skin twice per day or as directed by a physician. Rub in until completely absorbed. Apply to diseased or damaged nail tissue twice per day or as directed by a physician.


How Is Ure-K 50% Supplied



URE-K 50% cream (50% urea) is supplied in:

142g (5 oz) tube70350-2600-5

Storage And Handling



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


Principal Display Panel - 142 Gm Tube Label



NDC 70350-2600-5

FOR TOPICAL USE ONLY

URE-K 50%

50% UREA IN A CREAM BASE

Smooth
Easily Spreadable

Rx only

Solutech
PHARMACEUTICALS

Net WT. 5OZ (142 gm)


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