Video: Latest Treatment for Hep C.

Urea Solution

Pronunciation

Dosage Form: topical solution

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Urea 40% Nail Film
suspension with applicator

For external use only. Not for ophthalmic use.

Rx Only

Description: Urea 40% Nail Film is a keratolytic, emollient which is a gentle, yet potent, tissue softener for nails and skin.

Each gram of Urea 40% Nail Film suspension with applicator contains 40% urea, sodium hyaluronate disodium EDTA, glycerin, hydroxyethyl cellulose, PEG-6 caprylic/capric glycerides, purified water and xanthan gum.

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

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 purulent 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 or devitalized nails.

Contraindications: Known hypersensitivity to any of the listed ingredients.

Warnings: For external 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.

Pregnancy Category C: Animal reproduction studies have not been conducted with Urea 40% Nail Film. It is also not known whether Urea 40% Nail Film can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Urea 40% Nail Film 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 Urea 40% Nail Film is administered to a nursing woman.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

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

Dosage and Administration: Apply Urea 40% Nail Film to diseased or damaged nail tissue or skin twice per day, or as directed by a physician. Cover with adhesive bandage or gauze, secure with adhesive tape. An additional option is to remove a “finger” from a plastic or vinyl glove and slip it over the bandage-covered site. Secure glove finger with additional adhesive tape.

Slideshow: 29 Million And Counting - The Scourge of 21st Century America

How Supplied: Urea 40% Nail Film is supplied in a 18 mL glass bottle (NDC 42192-707-18) with an applicator brush.

Store at controlled room temperature 15° - 30°C (59° - 86°F). Protect from freezing.

All prescription substitutions using this product shall be made subject to state and federal statutes as applicable. Please note: this is not an Orange Book product and has not been subjected to FDA therapeutic equivalency or other equivalency testing. 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, incipients, inactive ingredients and chemical formulation information provided herein.

Manufactured for:
Acella Pharmaceuticals, LLC
Alpharetta, GA 30022
1-800-541-4802
Rev. 0413

PRINCIPAL DISPLAY PANEL- 18 mL

NDC 42192-707-18

Urea 40% Nail Film
suspension with appicator

For Topical Use Only
Not for Ophthalmic Use

Rx Only

Net Wt 18 mL

Acella
PHARMACEUTICALS, LLC

UREA 
Urea Solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:42192-707
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
UREA (UREA) UREA 400 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
HYALURONATE SODIUM  
EDETATE DISODIUM  
GLYCERIN  
HYDROXYETHYL CELLULOSE (6500 MPA.S AT 2%)  
PEG-6 CAPRYLIC/CAPRIC GLYCERIDES  
WATER  
XANTHAN GUM  
Packaging
# Item Code Package Description
1 NDC:42192-707-18 1 BOTTLE, WITH APPLICATOR (BOTTLE) in 1 CARTON
1 18 g in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 06/22/2009
Labeler - Acella Pharmaceuticals, LLC (825380939)
Revised: 04/2013
 
Acella Pharmaceuticals, LLC



More about urea topical

Consumer resources

Professional resources

Related treatment guides

Hide
(web1)