DESITIN MAXIMUM STRENGTH ZINC OXIDE DIAPER RASH- zinc oxide paste 
Kenvue Brands LLC

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Desitin ® Maximum Strength

40% Zinc Oxide Diaper Rash Paste

Drug Facts

Active ingredient

Zinc Oxide 40%

Purpose

Skin Protectant

Uses

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

Other information

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)

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

Principal Display Panel - 454 g Jar Label
DESITIN MAXIMUM STRENGTH ZINC OXIDE DIAPER RASH 
zinc oxide paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0396
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE400 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0396-1454 g in 1 JAR; Type 0: Not a Combination Product06/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01606/01/2018
Labeler - Kenvue Brands LLC (118772437)

Revised: 11/2024
Document Id: 26e03d32-1a19-2397-e063-6394a90a8982
Set id: 59728810-4ea9-45a1-b945-5a54199e01f3
Version: 5
Effective Time: 20241114
 
Kenvue Brands LLC