MAXIMUM STRENGTH MOISTURE BARRIER- petrolatum and zinc oxide ointment

Maximum Strength Moisture Barrier by

Drug Labeling and Warnings

Maximum Strength Moisture Barrier 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 50%

Zinc Oxide 16%

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

Directions

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

WARNINGS

Warnings

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

INACTIVE INGREDIENT

Aloe Barbadensis Flower Extract, DMDM Hydantoin; Hydrogenated Castor Oil; Myroxylon Balsamum, Vitamin A Palminate, Vitamin D, Vitamin E (Alpha Tocopherol)

PURPOSE

Skin Protectant

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

QUESTIONS

1-800-840-9041

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MAXIMUM STRENGTH MOISTURE BARRIER 
petrolatum and zinc oxide ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64772-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	0.5 g  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.16 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
VITAMIN D (UNII: 9VU1KI44GP)
MYROXYLON BALSAMUM WHOLE (UNII: 5OU0811D9J)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
DMDM HYDANTOIN (UNII: BYR0546TOW)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64772-203-01	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(64772-203) , label(64772-203)