Label: PURE CORNSTARCH BABY- corn starch powder

  • NDC Code(s): 0363-0911-15, 0363-0911-24
  • Packager: Walgreen Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 25, 2024

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  • ACTIVE INGREDIENT

    Active ingredient

    Corn Starch (Zea Mays) 99%

  • PURPOSE

    Purpose

    Skin Protectant

  • INDICATIONS & USAGE

    Uses

    • gently absorbs excess moisture for soft, dry skin.
    • helps protect against irritating friction, leaving your skin feeling cool and comfortable.
  • WARNINGS

    Warnings

    Avoid contact with eyes.

    For external use only.

    Do not use on broken skin.

    Keep powder away from child’s face to avoid inhalation, which can cause breathing problems.

    Close tightly after use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep this product out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    Shake powder into your hand and smooth onto skin.

  • STORAGE AND HANDLING

    Storage

    Store in a cool, dry place.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Tricalcium Phosphate, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl (Vitamin E).

  • SPL UNCLASSIFIED SECTION

    Package/Label Principal Display Panel

    Pure Cornstarch Baby Powder

    Gently absorbs excess moisture for soft, dry skin

    Clinically Tested

    NET WT 15 OZ (425 g)

  • 15 OZ Bottle Label

    Jar Label

  • 22 OZ Bottle Label

    Jar Label

  • INGREDIENTS AND APPEARANCE
    PURE CORNSTARCH BABY 
    corn starch powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0911
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STARCH, CORN (UNII: O8232NY3SJ) (STARCH, CORN - UNII:O8232NY3SJ) STARCH, CORN99 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0911-15425 g in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    2NDC:0363-0911-24624 g in 1 BOTTLE; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01607/17/2014
    Labeler - Walgreen Company (008965063)
    Registrant - Unipack LLC (116015769)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jell Pharmaceuticals Pvt. Ltd.726025211manufacture(0363-0911)
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