Friday, 31 August 2012

Umecta Nail Film



urea

Dosage Form: topical film
Umecta Nail Film

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 40% Nail Film suspension with applicator and pen applicator contains urea (40%), disodium EDTA, glycerin, hydroxyethylcellulose, PEG-6 caprylic/capric glycerides, purified water and xanthan gum.






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 Uses


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.





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 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 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 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 40% Nail Film suspension 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.

How Supplied


Umecta® 40% Nail Film (urea, 40%) suspension is available in a:


18 ml bottle - with applicator NDC 68712-010-01


Box of 6 - 3 ml - pen applicators NDC 68712-010-03


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   UREA
urea   film










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68712-010
Route of AdministrationTOPICALDEA Schedule    








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
















Inactive Ingredients
Ingredient NameStrength
Edetate Disodium 
Glycerin 
HYDROXYETHYL CELLULOSE (140 CPS AT 5%) 
CAPRYLIC/CAPRIC MONO/DIGLYCERIDES 
Water 
Xanthan Gum 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      


























Packaging
#NDCPackage DescriptionMultilevel Packaging
168712-010-0118 g In 1 BOTTLENone
268712-010-036 DOSE PACK In 1 CARTONcontains a DOSE PACK
23 g In 1 DOSE PACKThis package is contained within the CARTON (68712-010-03)
368712-010-0418 DOSE PACK In 1 CARTONcontains a DOSE PACK
33 g In 1 DOSE PACKThis package is contained within the CARTON (68712-010-04)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/01/2006


Labeler - Innocutis Holdings LLC (071501252)









Establishment
NameAddressID/FEIOperations
Ei Inc105803274manufacture
Revised: 11/2011Innocutis Holdings LLC

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Compare Umecta Nail Film with other medications


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