DESITIN MAXIMUM STRENGTH  ORIGINAL- zinc oxide ointment 
Johnson & Johnson Consumer Inc.

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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Desitin Maximum Strength Diaper Rash Paste

Drug Facts

Active ingredient(s)

Zinc Oxide 40%

Purposes

Skin Protectant

Uses

  • Helps treat and prevent diaper rash
  • Protects chafed skin due to diaper rash
  • 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 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 or soiled diapers promptly
  • Clean the diaper area
  • Allow to dry
  • Apply cream liberally as often as necessary, with each diaper change, especially at bedtime or any time prolonged exposure to wet diapers may be prolonged.

Other Information

Store at 20° to 25°C (68°F to 77°F)

Inactive ingredients

BHA, Cod Liver Oil, Fragrance, Lanolin, Methylparaben, Petrolatum, Talc, Water

Questions?

Call 1-800-720-3843 weekdays 9AM – 5PM EST

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

Desitin®
Maximum Strength   40% ZINC OXIDE
ORIGINAL PASTE   DIAPER RASH PASTE

MAXIMUM LEVEL
OF RASH-FIGHTING INGREDIENT

NET WT 4 Oz (113g)

  • HELPS HEAL, SOOTHE & PREVENT DIAPER RASH
Principal Display Panel - 113 g Tube Carton
DESITIN MAXIMUM STRENGTH   ORIGINAL
zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-0721
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
Butylated Hydroxyanisole (UNII: REK4960K2U)  
Cod Liver Oil (UNII: BBL281NWFG)  
Lanolin (UNII: 7EV65EAW6H)  
Methylparaben (UNII: A2I8C7HI9T)  
Petrolatum (UNII: 4T6H12BN9U)  
Talc (UNII: 7SEV7J4R1U)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58232-0721-03.5 g in 1 PACKET; Type 0: Not a Combination Product
2NDC:58232-0721-11 in 1 CARTON
228 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:58232-0721-21 in 1 CARTON
3113 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:58232-0721-31 in 1 CARTON
456 g in 1 TUBE; Type 0: Not a Combination Product
5NDC:58232-0721-41 in 1 CARTON
585 g in 1 TUBE; Type 0: Not a Combination Product
6NDC:58232-0721-51 in 1 CARTON
6136 g in 1 TUBE; Type 0: Not a Combination Product
7NDC:58232-0721-6454 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34709/08/201111/15/2017
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 11/2015
Document Id: 11b05197-c8af-4bff-abdc-a818b6fdda40
Set id: a6f12df6-ff76-4289-a687-5376666e94b8
Version: 2
Effective Time: 20151117
 
Johnson & Johnson Consumer Inc.