Wednesday, September 21, 2016

Umecta Mousse





Dosage Form: aerosol, foam
Umecta Mousse PI

Description


Rx only

For topical use only

Not for ophthalmic use


Umecta is a keratolytic, emollient which is a gentle, yet potent, tissue softener for nails and skin Each gram of Umecta Mousse contains urea (40%), Butane, Butyrospermum Parkii (Shea Butter) Extract, Carbomer, Glycine Soya (Soy Bean) Sterol, Helianthus Annuus (Sunflower) Oil, Isobutane, Laureth-4, Polysorbate-20, Propane, Purified Water, Stearic Acid, Triethanolamine. 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 and devitalized nails.



Contraindications


Known hypersensitivity to any of the listed ingredients.

Warnings


For external use only. Avoid contact with eyes, lips or mucous membranes. Umecta Mousse canister - contents under pressure do not puncture or incinerate. Do not store at temperatures above 120ยบ F.



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


Animal reproduction studies have not been conducted with Umecta. It is also not known whether Umecta can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. Umecta should be given to a pregnant woman only if clearly needed.

Nursing Monthers


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 Umecta 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 Umecta PD bioadhesive emulsion/topical suspension or Umecta Mousse to affected skin twice per day, or as directed by a physician. Rub in until completely absorbed



How Supplied


Umecta (urea, 40%) mousse is available in a: 4 oz. can NDC 68712-020-01


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


Protect from freezing.


Manufactured for:


Innocutis Holdings LLC

Charleston, SC 29401

Toll Free: 1-800-499-4468

www.innocutis.com

www.umecta.com
















Umecta Mousse  UREA
urea foam  aerosol, foam










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68712-020
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
UREA (UREA)UREA400 mg  in 1 g




























Inactive Ingredients
Ingredient NameStrength
BUTANE 
SHEA BUTTER 
CARBOMER 934 
SOYBEAN OIL 
SUNFLOWER OIL 
ISOBUTANE 
LAURETH-4 
POLYSORBATE 20 
PROPANE 
WATER 
STEARIC ACID 
TROLAMINE 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
168712-020-01113.4 g In 1 CANNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/01/2007


Labeler - Innocutis Holdings LLC (071501252)









Establishment
NameAddressID/FEIOperations
American Spraytech LLC137135237manufacture
Revised: 12/2011Innocutis Holdings LLC

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