MOISTURE BARRIER CREAM- petrolatum, zinc oxide cream

Moisture Barrier Cream by

Drug Labeling and Warnings

Moisture Barrier Cream by is a Otc medication manufactured, distributed, or labeled by Derma Sciences Canada Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Petrolatum 23%

Zinc Oxide 4.1 %

PURPOSE

Skin Protectant

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INACTIVE INGREDIENT

Beeswax, Cetostearyl Alcohol, Hydrogenated Castor Wax, lmidazolidinyl Urea, Methylparaben, Mineral Oil, Paraffin, Propylparaben, Sodium Cl1Ioride, Vitamin A Palmitate, Vitamin D, Vitamin E (Alpha Tocopherol), Water

WARNINGS

Warnings Keep out of reach of children For external use only Avoid eye contact. Discontinue use and contact a physician if condition worsens

ASK DOCTOR

Discontinue use and contact a physician if condition worsens

INDICATIONS & USAGE

Uses: Temporarily protects and helps relieve minor skin irritation and itching due to rashes.

DOSAGE & ADMINISTRATION

Carefully cleanse the area and pat dry thoroughly. Apply liberally to desired areas often as necessary.

QUESTIONS

1-800-840-9041

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOISTURE BARRIER CREAM 
petrolatum, zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64772-204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	0.23 g  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.041 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PARAFFIN (UNII: I9O0E3H2ZE)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
METHYLPARABEN (UNII: A2I8C7HI9T)
IMIDAZOLIDINYL UREA (UNII: M629807ATL)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
VITAMIN D (UNII: 9VU1KI44GP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MINERAL OIL (UNII: T5L8T28FGP)
BEESWAX (UNII: 2ZA36H0S2V)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64772-204-01	113.4 g in 1 TUBE; Type 0: Not a Combination Product	11/13/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/13/2014

Labeler - Derma Sciences Canada Inc. (200564891)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Sciences Canada Inc.		200564891	manufacture(64772-204) , label(64772-204)