KERAFOAM - urea aerosol, foam 
Onset Dermatologics LLC

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.

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DESCRIPTION:

KERAFOAM® Emollient Foam is a keratolytic emollient foam which is a tissue softener for skin and/or nails. KERAFOAM Emollient Foam contains 30% urea USP in an aqueous based emollient foam vehicle. Each gram of KERAFOAM Emollient Foam contains 30% urea USP, ammonium lactate, cetyl alcohol NF, emulsifying wax NF, methylparaben NF, propylene glycol USP, propylparaben NF, purified water USP, steareth-10. Also contains: Propellant HFA-134a (1,1,1,2-tetrafluoroethane).
Urea USP is a diamide of carbonic acid with the following chemical structure:

K42 Chemical Structure

CLINICAL PHARMACOLOGY

Urea gently lyses/dissolves the intercellular matrix of surface skin cells loosening and allowing a shedding of rough, thickened and scaly hyperkeratotic skin. Urea also moisturizes and softens skin.

INDICATIONS

For softening, smoothing and removing rough scaling hyperkeratotic skin in conditions such as xerosis, ichthyosis, skin cracks and fissures, dermatitis, eczema, psoriasis, keratoses and calluses.

CONTRAINDICATIONS

Known hypersensitivity to any of the listed ingredients. Discontinue use if hypersensitivity is observed.

WARNINGS

FOR EXTERNAL USE ONLY. Avoid contact with eyes, lips or mucous membranes. Keep out of the reach of children. Contents under pressure. Do not puncture or incinerate container. Do not expose to temperatures above 120ºF (49ºC).

PRECAUTIONS

Information for patients:

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

Pregnancy Category C. Animal reproduction studies have not been conducted with KERAFOAM Emollient Foam. It is not known whether KERAFOAM Emollient Foam can cause fetal harm when administered to a  pregnant woman or can affect reproduction capacity. KERAFOAM Emollient Foam 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 KERAFOAM Emollient Foam is administered to a nursing woman.

ADVERSE REACTIONS

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

DOSAGE AND ADMINISTRATION


Shake Vigorously, Tap Bottom of Can, and Prime Before Initial Use. Shake Vigorously and Tap Before Each Use.
To Prime: After shaking, gently tap bottom of can onto palm of other hand or a solid surface at least 3 times. Hold the can upright, direct away from the patient, and firmly depress the actuator for 1 to 3 seconds or until foam begins to dispense. (If foam does not dispense within 3 seconds: re-shake can, gently tap bottom of can onto a solid surface at least 3 times, and depress the actuator again until foam begins to dispense.)
Before Each Use: Shake vigorously and gently tap bottom of can onto palm of other hand or a solid surface at least 3 times.
During Use: Holding can upright, dispense KERAFOAM into palm of hand and apply to affected area twice per day, or as directed by a physician. Rub in until completely absorbed. Wipe off any excess foam from actuator after use.

HOW SUPPLIED

KERAFOAM Emollient Foam is supplied in a 60 g (NDC# 16781-157-60) aluminum can.

Store at room temperature: 59º - 77ºF (15º - 25ºC). Protect from freezing. Store upright.

Patent Pending

P/N 2604 Rev. 3

Manufactured For:

Onset Logo

Onset Therapeutics
Cumberland, RI 02864

(888) 713-8154
www.onsettx.com

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - Kerafoam Outer Carton - 5g

NDC 16781-157-06
Rx Only

Kerafoam®
Emollient Foam
Urea (30%)

For softening, smoothing, and removing rough scaling hyperkeratotic skin
See prescribing information enclosed

Kerafoam Outer Carton - 5g

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - Kerafoam Inner Label - 5g

NDC 16781-157-06
Rx Only
Professional Sample
Not for Sale
Net Weight 5g

Kerafoam®
Emollient Foam
Urea (30%)

Sample will not dispense entire contents.

Kerafoam_Inner_Label_5g



KERAFOAM 
urea aerosol, foam
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:16781-157
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
UREA (UREA) UREA30 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
AMMONIUM LACTATE 
PROPYLENE GLYCOL 
CETYL ALCOHOL 
PROPYLPARABEN 
METHYLPARABEN 
WATER 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMultilevel Packaging
1NDC:16781-157-066 CAN (1 CAN) in 1 BOXcontains a CAN
15 g in 1 CANThis package is contained within the BOX (16781-157-06)
2NDC:16781-157-116 CAN (1 CAN) in 1 BOXcontains a CAN
210 g in 1 CANThis package is contained within the BOX (16781-157-11)
3NDC:16781-157-601 CAN (1 CAN) in 1 BOXcontains a CAN
360 g in 1 CANThis package is contained within the BOX (16781-157-60)
4NDC:16781-157-961 CAN (1 CAN) in 1 BOXcontains a CAN
4100 g in 1 CANThis package is contained within the BOX (16781-157-96)

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other12/01/2006

Labeler - Onset Dermatologics LLC (793223707)
Registrant - Onset Dermatologics LLC (964275155)
Establishment
NameAddressID/FEIOperations
Onset Dermatologics LLC793223707Manufacture

Revised: 06/2011 Onset Dermatologics LLC