UP AND UP CREAMY DIAPER RASH (ZINC OXIDE) OINTMENT [TARGET CORPORATION]

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UP AND UP CREAMY DIAPER RASH (ZINC OXIDE) OINTMENT [TARGET CORPORATION]
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NDC 11673-332-04
Set ID f8a2e3d7-18a5-47bb-9016-ba063e05b9b3
Category HUMAN OTC DRUG LABEL
Packager TARGET CORPORATION
Generic Name
Product Class
Product Number
Application Number PART346
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  • ACTIVE INGREDIENT

    ZINC OXIDE 13%

    PURPOSE

    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

    AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.

    STOP USING THIS PRODUCT AND ASK A DOCTOR IF

    CONDITION WORSENS OR DOES NOT IMPROVE WITHIN 7 DAYS.

    KEEP OUT OF REACH OF CHILDREN

    IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

  • DIRECTIONS

    CHANGE WET AND SOILED DIAPERS PROMPTLY. CLEAN THE DIAPER AREA AND ALLOW TO DRY. APPLY OINTMENT LIBERALLY AS OFTEN AS REQUIRED WITH EACH DIAPER CHANGE, ESPECIALLY AT BEDTIME OR ANYTIME WHEN EXPOSURE TO WET DIAPERS MAY BE PROLONGED.

  • OTHER INFORMATION

    STORE BETWEEN 20-25C (68-77F).

  • INACTIVE INGREDIENTS:

    ALOE BARBADENSIS LEAF JUICE, BEESWAX, DIMETHICONE, ETHYLHEXYLGLYCERIN, FRAGRANCE (PARFUM), MAGNESIUM SULFATE, MICROCRYSTALLINE WAX, MINERAL OIL, PEG-30 DIPOLYHYDROXYSTEARATE, PETROLATUM, PHENOXYETHANOL, POTASSIUM HYDROXIDE, SORBITAN SESQUIOLEATE, TOCOPHERYL ACETATE, WATER (AQUA).

  • QUESTIONS?

    CALL 1-800-910-6874

  • LABEL COPY

    IMAGE OF THE LABEL

  • INGREDIENTS AND APPEARANCE
    UP AND UP  CREAMY DIAPER RASH
    zinc oxide ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-332
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE13.0 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    APIS MELLIFERA (UNII: 7S82P3R43Z)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-332-04113.3 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34604/23/2012
    Labeler - TARGET CORPORATION (006961700)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture
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