Label: DRY IDEA STRESS SHIELD INSPIRE ANTIPERSPIRANT DEODORANT ROLL-ON- aluminum zirconium pentachlorohydrex gly liquid

  • NDC Code(s): 54565-2904-1
  • Packager: KDC/ONE Development Corporation, Inc
  • 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 August 18, 2021

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Aluminum Zirconium Pentachlorohydrex Gly 16.3%

  • PURPOSE

    USE....Reduces underarm perspiration - Extra effective

  • WARNINGS

    Warnings...For external use only.

  • DO NOT USE

    Do not use on broken skin.

  • STOP USE

    Stop use and ask a doctor is rash or irritation occurs.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.  If swallowed, get medical help or contact a poison control center right away.

  • ASK DOCTOR

    Ask a doctor before use if you have kidney disease.

  • INDICATIONS & USAGE

    Directions: Shake well. Apply to underarms only.

  • INACTIVE INGREDIENT

    Inactive Ingredients;  Cyclomethicone, Disteardimonium Hectorite, Propylene Carbonate, Gossypium Herbaceum (Cotton) Seed Oil, Tocopheryl Acetate (Vitamin E Acetate), Isopropyl Myristate, Fragrance, Zea Mays (Corn) Starch.

  • QUESTIONS

    Questions: 1-800-258-DIAL

  • HOW SUPPLIED

    2017 Distributed By The Dial Corporation, Scottsdale, AZ 85255. Henkel Corporation, Rocky Hill, CT 06067.

  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Shake well. Apply to underarms only.

  • PRINCIPAL DISPLAY PANEL

    DI_Inspire

  • INGREDIENTS AND APPEARANCE
    DRY IDEA STRESS SHIELD INSPIRE ANTIPERSPIRANT DEODORANT ROLL-ON 
    aluminum zirconium pentachlorohydrex gly liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54565-2904
    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 96.1 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54565-2904-196.1 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/30/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35010/07/2014
    Labeler - KDC/ONE Development Corporation, Inc (204006464)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC/ONE Development Corporation, Inc204006464manufacture(54565-2904) , analysis(54565-2904) , pack(54565-2904) , label(54565-2904)