Label: DRY IDEA ADVANCED DRY ROLL-ON ANTIPERSPIRANT AND DEODORANT UNSCENTED liquid

  • NDC Code(s): 82699-202-03, 82699-202-04
  • Packager: Thriving Brands LLC
  • 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 September 28, 2023

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  • DOSAGE & ADMINISTRATION

    Dosage & Administration Section

  • ACTIVE INGREDIENT

    OTC-Active Ingredient Section

  • ASK DOCTOR

    OTC-Ask Doctor Section

  • KEEP OUT OF REACH OF CHILDREN

    OTC-Keep out of reach of children section

  • PURPOSE

    OTC-Purpose Section

  • STOP USE

    OTC-Stop Use Section

  • INDICATIONS & USAGE

    Indications & Usage Section

  • WARNINGS

    Warnings

  • INACTIVE INGREDIENT

    Inactive Ingredient Section

  • PRINCIPAL DISPLAY PANEL

    Package Label Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    DRY IDEA ADVANCED DRY ROLL-ON ANTIPERSPIRANT AND DEODORANT UNSCENTED 
    dry idea advanced dry roll-on antiperspirant and deodorant unscented liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82699-202
    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 96 mL
    Inactive Ingredients
    Ingredient NameStrength
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    Product Characteristics
    Colorbrown (Light) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82699-202-0396 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product07/03/2023
    2NDC:82699-202-04192 mL in 1 PACKAGE; Type 0: Not a Combination Product07/03/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM01907/03/2023
    Labeler - Thriving Brands LLC (118346160)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC/One Development Corporation, Inc204006464manufacture(82699-202) , pack(82699-202) , label(82699-202) , analysis(82699-202)