DIAPER RASH- zinc oxide ointment 
United Natural Foods, Inc. dba UNFI

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Diaper Rash Ointment 40% Zinc Oxide
020.002/020AC-AD

Active ingredients

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 soilded 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 1-877-932-7948

Disclaimer

This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Destin Maximum Strength Diaper Rash Paste.

Adverse Reactions 

DISTRIBUTED BY SUPERVALU, INC

EDEN PRAIRIE, MN 55344

www.supervalu-ourownbrands.com

Principal display panel

NDC 41163-820-26

Baby basics

Compare to Desitin Maximum Strength Diaper Rash Paste active ingredient*

Zinc Oxide

Diaper Rash Ointment

Skin Protectant

  • Helps Promote Healting
  • Protects chafed skin
  • Hypoallergenic

NET WT 4 OZ (113 g)

image description

DIAPER RASH 
zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-020
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)  
starch, corn (UNII: O8232NY3SJ)  
glycerin (UNII: PDC6A3C0OX)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41163-020-261 in 1 CARTON11/18/2009
1113 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34711/18/2009
Labeler - United Natural Foods, Inc. dba UNFI (943556183)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(41163-020)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(41163-020)

Revised: 5/2023
Document Id: 172815a1-b778-4ab0-8d58-3faf72f5bef6
Set id: 014d0028-486e-4f1c-a14f-8162e393ebca
Version: 14
Effective Time: 20230516
 
United Natural Foods, Inc. dba UNFI