Label: DESITIN MAXIMUM STRENGTH DIAPER RASH- zinc oxide paste

  • NDC Code(s): 69968-0061-1, 69968-0061-2, 69968-0061-3, 69968-0061-4, view more
    69968-0061-5, 69968-0061-7, 69968-0061-9
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2023

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  • 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, beeswax, tocopheryl acetate, fragrance

  • Questions?

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

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    JOHNSON & JOHNSON CONSUMER INC.
    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 113 g Tube Carton

    #1 CHOICE OF PEDIATRICIANS & MOMS

    Desitin ®
    Maximum Strength     		 
    provides powerful,
    long-lasting relief

    •    Paraben-free        Zinc Oxide Diaper Rash Paste        NET WT 4 Oz (113 g)

    PRINCIPAL DISPLAY PANEL - 113 g Tube Carton
  • INGREDIENTS AND APPEARANCE
    DESITIN MAXIMUM STRENGTH DIAPER RASH 
    zinc oxide paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0061
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0061-11 in 1 CARTON11/16/2015
    128 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:69968-0061-21 in 1 CARTON11/16/2015
    257 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:69968-0061-41 in 1 CARTON11/16/2015
    3113 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:69968-0061-51 in 1 CARTON11/16/2015
    4136 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:69968-0061-9454 g in 1 JAR; Type 0: Not a Combination Product11/16/2015
    6NDC:69968-0061-33 in 1 CARTON11/16/2015
    6136 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:69968-0061-73.5 g in 1 POUCH; Type 0: Not a Combination Product11/16/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/16/2015
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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