DESITIN MAXIMUM STRENGTH ZINC OXIDE DIAPER RASH- zinc oxide paste

Desitin Maximum Strength Zinc Oxide Diaper Rash by

Drug Labeling and Warnings

Desitin Maximum Strength Zinc Oxide Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Zinc Oxide 40%

Purpose

Skin Protectant

Uses

• helps treat and prevent diaper rash
• protects chafed skin due to 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 paste 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 at 20°C to 25°C (68°F to 77°F)
• may stain clothing

Inactive ingredients

petrolatum, cod liver oil, lanolin, talc, glycerin, sorbitan sesquioleate, penta erithrityl tetra-di-t-butyl hydroxyhydrocinnamite, beeswax, tocopheryl acetate, fragrance

Questions?

Call toll-free 800-720-3843 or 215-273-8755 (collect)

SPL UNCLASSIFIED SECTION

Distributed in the U.S. by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 454 g Jar Label

#1 CHOICE OF PEDIATRICIANS
& PARENTS

Desitin®
Maximum Strength
40% Zinc Oxide Diaper Rash Paste

soothes and relieves on contact
clinically proven, long-lasting relief

Free from parabens, phthalates, and dyes
Hypoallergenic . Pediatrician & Dermatologist tested

• NET WT 1 lb
  16 Oz (454 g)

INGREDIENTS AND APPEARANCE

DESITIN MAXIMUM STRENGTH ZINC OXIDE DIAPER RASH 
zinc oxide paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0396
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	400 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Petrolatum (UNII: 4T6H12BN9U)
Cod Liver Oil (UNII: BBL281NWFG)
Lanolin (UNII: 7EV65EAW6H)
Talc (UNII: 7SEV7J4R1U)
Glycerin (UNII: PDC6A3C0OX)
Sorbitan Sesquioleate (UNII: 0W8RRI5W5A)
YELLOW WAX (UNII: 2ZA36H0S2V)
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0396-1	454 g in 1 JAR; Type 0: Not a Combination Product	06/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	06/01/2018

Labeler - Johnson & Johnson Consumer Inc. (002347102)