Label: SOFT AND DRI DRIGEL- aluminum zirconium octocholrohydrex 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 December 20, 2019

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  • Active Ingredient

    Aluminum Zirconium Octachlorohydrex Gly (16.4%)

  • PURPOSE

    Antiperspirant

  • Use

    reduces underarm perspiration

  • Warnings For external use only

    Stop use and ask a doctor if

    rash or irritation occurs

    Keep out of reach of chlidren

    If swallowed, get medical help or contact a posion control center right away

    Ask a doctor before use if

    you have kidney disease

    Do not use

    on broken skin

  • Directions

    Apply to underarms only.

  • DOSAGE & ADMINISTRATION

    Apply to underarms only.

  • Inactive ingredients

    Water, ( Auqua, EAU), Alcohol denat., Cyclopentsiloxane, Propylene Glycol, Dimethicone, Calcium cholride, Trisiloxane, Pentasiloxane, PEG/PPG-18/18, Dimethicone, T-butyl alcohol, Denaton-ium Benzoate, Fragrance (Parfum), Benzyl Salicylate, Cirtronellol, Benzyl Alcohol, Geraniol, Limonene

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    SOFT AND DRI DRIGEL 
    aluminum zirconium octocholrohydrex stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69752-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY - UNII:P9D3YP29MY) ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY164 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69752-102-061 in 1 TUBE11/13/2015
    185 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35011/13/2015
    Labeler - The Village Company (172208105)
    Registrant - Apex International (015226132)
    Establishment
    NameAddressID/FEIBusiness Operations
    VVF024177178manufacture(69752-102)
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