Label: SUNSCREEN- zinc oxide sunscreen stick

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated January 4, 2022

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  • Tubby Todd Play Mineral Sunstick Dosage & Administration

    Dosage

  • Tubby Todd Play Mineral Sunstick, Warnings

    Warnings

  • Tubby Todd Play Mineral Sunstick Inactive ingredients

    Inactive Ingredients

  • INDICATIONS & USAGE

    Indications and Usage

  • Tubby Todd Play Mineral Sunstick Keep out of Reach

    Keep Out of Reach

  • PURPOSE

    Purpose

  • ACTIVE INGREDIENT

    Active Ingredients

  • Tubby Todd Label for Container

    Artwork

  • Tubby Todd Unit Carton

    Unit Carton

  • INGREDIENTS AND APPEARANCE
    SUNSCREEN 
    zinc oxide sunscreen stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62932-202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)  
    .GAMMA.-TOCOPHEROL (UNII: 8EF1Z1238F)  
    .DELTA.-TOCOPHEROL (UNII: JU84X1II0N)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .BETA.-TOCOPHEROL (UNII: 9U6A490501)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62932-202-341 in 1 CARTON04/01/2019
    114 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35204/01/2019
    Labeler - Private Label Select Ltd CO (005415463)
    Registrant - Private Label Select Ltd CO (005415463)
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