Label: GILLETTE CLINICAL PROTECTION COOL WAVE CLEAR- aluminum zirconium octachlorohydrex gly gel

  • NDC Code(s): 69423-584-45, 69423-584-73
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 4, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum zirconium octachlorohydrex Gly 20% (anhydrous)

  • Purpose

    Antiperspirant

  • Use

    reduces underarm wetness

  • Warnings

    For external use only.

    Do not use on broken skin

    Ask a doctor before use if you have kidney disease

    Stop use if rash or irritation occurs

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • apply to underarms only
    • apply 3 - 4 clicks of product to underarms at bedtime
    • rub in until clear
  • Inactive ingredients

    water, cyclopentasiloxane, dimethicone, propylene glycol, alcohol denat., calcium chloride, PEG/PPG-18/18 dimethicone, fragrance

  • Questions?

    1-800-445-5388

  • SPL UNCLASSIFIED SECTION

    Dist. by PROCTER & GAMBLE,
    CINCINNATI, OH 45202.

  • PRINCIPAL DISPLAY PANEL - 45 g Canister Carton

    Gillette®

    CLINICAL

    PROTECTION

    72 HR

    EXTREME

    SWEAT PROTECTION

    COOL WAVE
    CLEAR GEL

    ALUMINUM ZIRCONIUM

    OCTACHLOROHYDREX GLY
    ANTI-PERSPIRANT/DEODORANT

    NET WT. 1.6 OZ. (45 g)

    Gill

  • INGREDIENTS AND APPEARANCE
    GILLETTE CLINICAL PROTECTION COOL WAVE CLEAR 
    aluminum zirconium octachlorohydrex gly gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-584
    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 GLY20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    TETRAHYDROLINALYL ACETATE (UNII: 2NDV3959AX)  
    ORANGE TERPENES (UNII: 9J3RG7FX7S)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    ALCOHOL (UNII: 3K9958V90M)  
    TETRAHYDROLINALOOL (UNII: UM4XS5M134)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    COUMARIN (UNII: A4VZ22K1WT)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    DIHYDROMYRCENOL (UNII: 46L1B02ND9)  
    LINALYL ACETATE (UNII: 5K47SSQ51G)  
    CITRAL (UNII: T7EU0O9VPP)  
    CITRONELLYL NITRILE, (+/-)- (UNII: GP9AT16H16)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)  
    ALLYL AMYL GLYCOLATE (UNII: EMX89K493E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-584-451 in 1 CARTON01/01/2021
    145 g in 1 CANISTER; Type 0: Not a Combination Product
    2NDC:69423-584-731 in 1 CARTON01/01/2021
    273 g in 1 CANISTER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/01/2021
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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