DR. WALTONS BABY POWDER (TALC) POWDER [DR. WALTONS, INCORPORATED]

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  • DR. WALTONS BABY POWDER (TALC) POWDER [DR. WALTONS, INCORPORATED]

DR. WALTONS BABY POWDER (TALC) POWDER [DR. WALTONS, INCORPORATED]
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NDC 76271-001-02, 76271-001-24
Set ID 4c0dac58-34b5-418a-a54c-5ffcb690771f
Category HUMAN OTC DRUG LABEL
Packager Dr. Waltons, Incorporated
Generic Name
Product Class
Product Number
Application Number PART347
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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF CHILDREN'S REACH. AVOID BABY'S EYES, NOSE AND MOUTH.

  • PURPOSE

    GREAT FOR YOUR BABY: PREVENTS AND SOOTHES DIAPER RASH, ELIMINATES ODOR. USE AFTER EVERY BATH AND DIAPER CHANGE.

    GREAT FOR YOU: USE DAILY FOR SOFT, IRRITATION-FREE SKIN. REDUCES CHAFING AND ABSORBS MOISTURE. GREAT FOR ELIMINATING SAND AND MOISTURE AFTER A DAY AT THE BEACH!


  • DO NOT USE

    CAUTION: KEEP OUT OF CHILDREN'S REACH. AVOID BABY'S EYES, NOSE AND MOUTH. NOT FOR USE ON BROKEN SKIN. IF IRRITATION DEVELOPS, PLEASE DISCONTINUE USE.

    HYPOALLERGENIC; DERMATOLOGIST AND ALLERGY TESTED; PEDIATRICIAN TESTED

  • WARNINGS

    IF IRRITATION DEVELOPS, PLEASE DISCONTINUE USE.

  • INDICATIONS & USAGE

    PREVENTS AND SOOTHES DIAPER RASH, ELIMINATES ODOR

  • DOSAGE & ADMINISTRATION

    SHAKE POWDER ONTO HANDS AND GENTLY RUB ONTO SKIN

  • INACTIVE INGREDIENT

    TALC

  • ACTIVE INGREDIENT

    VITAMIN E (ALPHA-TOCOPHEROL), ZINC OXIDE

  • PRINCIPAL DISPLAY PANEL

    image of front label image of back labelEnter section text here

  • INGREDIENTS AND APPEARANCE
    DR. WALTONS   BABY POWDER
    talc powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76271-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) (ALPHA-TOCOPHEROL - UNII:H4N855PNZ1) ALPHA-TOCOPHEROL5.2 g  in 675 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE5.13 g  in 675 g
    Inactive Ingredients
    Ingredient NameStrength
    TALC (UNII: 7SEV7J4R1U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76271-001-24675 g in 1 BOTTLE, PLASTIC
    2NDC:76271-001-0255 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34707/09/2011
    Labeler - Dr. Waltons, Incorporated (041377104)
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