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Desitin Maximum Strength Diaper Rash

Medically reviewed on October 27, 2016

Dosage form: paste
Ingredients: Zinc Oxide 400mg in 1g
Labeler: Johnson & Johnson Consumer Inc.
NDC Code: 58232-9927

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.

Desitin Maximum Strength Diaper Rash

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 day

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 cream 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° to 25°C (68° to 77°F)
  • May stain clothing

Inactive ingredients

Petrolatum
Cod Liver Oil
Lanolin
Talc
Glycerin
Sorbitan Sesquioleate
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 PRODUCTS COMPANY

Division of Johnson & Johnson
Consumer Companies, Inc.
Skillman, NJ 08558-9418

PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

#1 CHOICE OF PEDIATRICIANS & MOMS

NEW FORMULA

Desitin®
Maximum Strength

provides powerful,
long-lasting relief
  • Paraben-free
Zinc Oxide Diaper Rash PasteNET WT 4 Oz (113 g)
DESITIN MAXIMUM STRENGTH DIAPER RASH 
zinc oxide paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-9927
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (Zinc Oxide) Zinc Oxide400 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Petrolatum 
Cod Liver Oil 
Lanolin 
Talc 
Glycerin 
Sorbitan Sesquioleate 
Yellow Wax 
.Alpha.-Tocopherol Acetate 
Packaging
#Item CodePackage Description
1NDC:58232-9927-03.5 g in 1 PACKET
2NDC:58232-9927-11 TUBE in 1 CARTON
228 g in 1 TUBE
3NDC:58232-9927-21 TUBE in 1 CARTON
357 g in 1 TUBE
4NDC:58232-9927-41 TUBE in 1 CARTON
4113 g in 1 TUBE
5NDC:58232-9927-51 TUBE in 1 CARTON
5136 g in 1 TUBE
6NDC:58232-9927-9454 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34711/16/201510/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

 
Johnson & Johnson Consumer Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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