DIAPER RASH- zinc oxide paste

Diaper Rash by

Drug Labeling and Warnings

Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Target Corporation, Vi Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Zinc oxide  40%

Purpose

Skin Protectant

Uses

helps treat and prevent diaper rash
protects chafed skin due to the diaper rash and helps seal out wetness

Warnings

For external use only

When using this product

• do not get into eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• change wet and soiled diapers promptly
• cleanse the diaper area
• allow to dry
• apply ointment liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged

Other information

store between 20⁰ and 25⁰C (68⁰ and 77⁰F)

inactive ingredients

petrolatum, cod liver oil, lanolin, Zea mays (corn) starch, glycerin, sorbitan sesquioleate, beeswax, tocopheryl acetate, fragrance

questions

Call 1-800-910-6874

claims

This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Destine Maximum Strength

40% Zinc Oxide Diaper Rash Paste.

Adverse Reactions

Distributed by Target Corporation

Minneapolis, MN 55403

Made in the U.S.A. with U.S.A and foreign components

2016 Target Brands, Inc.  Shop Target.com

020.002/020AC

principal display panel

NDC: 11673-809-26

Compare to Desitin

Maximum Strength 40% Zinc

Oxide Diaper Rash Paste

maximum  strength

diaper rash

paste

40% zinc oxide

skin protectant

pediatrician tested

seals out wetness

hypoallergenic

paraben free

up & up

NET WT 4 OZ (113.3 g)

INGREDIENTS AND APPEARANCE

DIAPER RASH 
zinc oxide paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	532 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
COD LIVER OIL (UNII: BBL281NWFG)
LANOLIN (UNII: 7EV65EAW6H)
STARCH, CORN (UNII: O8232NY3SJ)
GLYCERIN (UNII: PDC6A3C0OX)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
YELLOW WAX (UNII: 2ZA36H0S2V)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-020-26	1 in 1 PACKAGE	03/24/2008
1		113.3 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 11673-020-43	1 in 1 PACKAGE	03/24/2008
2		453.5 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	03/24/2008

Labeler - Target Corporation (006961700)

Registrant - Vi Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi Jon		790752542	manufacture(11673-020)