Label: AXE NIGHT ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray

  • NDC Code(s): 64942-1373-1, 64942-1373-2
  • Packager: Conopco Inc. d/b/a Unilever
  • 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 30, 2020

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  • ACTIVE INGREDIENT

    Active ingredient

    Aluminum chlorohydrate (23.3%)

  • PURPOSE

    Purpose

    anti-perspirant

  • INDICATIONS & USAGE

    Uses
    · reduces underarm wetness

  • WARNINGS

    WARNINGS

    For external use only

    • FLAMMABLE.  DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING.  CAN CAUSE SERIOUS INJURY OR DEATH.
    • Keep away from face and mouth to avoid breathing in.
    • Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120 degrees F/50 degrees C or in enclosed places that could overheat.
    • Do not use on broken skin. Stop use if rash or irritation occurs.
    • Ask a doctor before using if you have kidney disease.
    • USE ONLY AS DIRECTED.  INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING  AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL. Help stop inhalation abuse.  For information visit www.inhalant.org

    • KEEP OUT OF REACH OF CHILDREN

  • DOSAGE & ADMINISTRATION

    Directions  Apply to underarms only.  If dispenser clogs, rinse in warm water.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Propylene Carbonate

  • QUESTIONS

    Questions?
    Call toll-free 1-800-450-7580

  • 3.8 oz PDP

    AxeNightDrySprayAPPDP

  • INGREDIENTS AND APPEARANCE
    AXE  NIGHT ANTIPERSPIRANT
    aluminum chlorohydrate aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1373
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE23.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BUTANE (UNII: 6LV4FOR43R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ISOBUTANE (UNII: BXR49TP611)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    PROPANE (UNII: T75W9911L6)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1373-1107 g in 1 CAN; Type 0: Not a Combination Product11/01/2014
    2NDC:64942-1373-228 g in 1 CAN; Type 0: Not a Combination Product11/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35011/01/2014
    Labeler - Conopco Inc. d/b/a Unilever (001375088)
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