Label: DRY IDEA ADVANCED DRY ANTIPERSPIRANT ROLL-ON, POWDER FRESH liquid

  • NDC Code(s): 82699-201-03, 82699-201-04
  • Packager: Thriving Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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    Warnings Section

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    Indications & Usage Section

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    Dosage & Administration Section

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    Inactive Ingredient Section

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    OTC-Active Ingredient Section

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    OTC-Ask Doctor Section

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    OTC-Ask Doctor/Pharmacist Section

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    OTC-Do Not Use Section

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    OTC-Keep Out of Reach of Children Section

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    OTC-Pregnancy or Breast Feeding Section

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    OTC-Purpose Section

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    OTC-Questions Section

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    OTC-Stop Use Section

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    OTC-When Using Section

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    Package Label.Principal Display PanelPackage Label.Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    DRY IDEA ADVANCED DRY ANTIPERSPIRANT ROLL-ON, POWDER FRESH 
    dry idea advanced dry antiperspirant roll-on, powder fresh liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82699-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY (UNII: 94703016SM) (ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY - UNII:94703016SM) ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY16.3 g  in 16.3 g
    Inactive Ingredients
    Ingredient NameStrength
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    Product Characteristics
    Colorbrown (Light Brown) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82699-201-0396.1 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/31/2023
    2NDC:82699-201-04576.6 g in 1 PACKAGE; Type 0: Not a Combination Product09/28/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01903/31/2023
    Labeler - Thriving Brands LLC (118346160)