FDA Label for Urea
View Indications, Usage & Precautions
Urea Product Label
The following document was submitted to the FDA by the labeler of this product Akron Pharma Inc. 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.
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: Purified Water, Propylene Glycol, Glyceryl Monostearate, Mineral Oil, Cetyl Alcohol, Phosphomer X-Polymer, Trolamine 99% , White Petrolatum, Xanthan Gum.
Urea is a diamide of carbonic acid with the following chemical structure:
Clinical Pharmacology
Urea gently dissolves the intracellular matrix which results in loosening of the horny layer of the skin and shedding of scaly skin at regular intervals, thereby softening hyperkeratotic areas of the skin.
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 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
Known hypersensitivity to any of the listed ingredients.
Warnings
For topical use only. Avoid contact with eyes, lips or mucous membranes.
Precautions
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.
Adverse Reactions
Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the medication.
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.
How Supplied
Urea Lotion 40% 8 oz. (226.8g): NDC 71399-8455-8
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.
All prescription substitutions using this product shall be made subject to state and federal statutes
as applicable. NOTE: this is not an Orange Book product and has not been subjected to FDA
therapeutic equivalency or other equivalency testing. No representation is made as to generic
status or bioequivalency. Each person recommending a prescription substitution using this product
shall make such recommendations based on each such person’s professional opinion and
knowledge, upon evaluating the active ingredients, excipients, inactive ingredients and chemical
formulation information provided herein.
QUESTIONS :
Please Call 1(877) 225-6999
Manufactured for:
Akron Pharma, Inc, Fairfield, NJ 07004
Manufactured in U.S.A
Package Label.Principal Display Panel
* Please review the disclaimer below.