Label: AXE- phoenix dry spray antiperspirant 48hr protection dry aerosol, spray

  • NDC Code(s): 64942-1570-1
  • 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 December 1, 2021

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  • AXE PHOENIX DRY SPRAY ANTIPERSPIRANT 48HR PROTECTION DRY - aluminum chlorohydrate aerosol, spray

    Axe Phoenix Dry Spray Antiperspirant 48HR Protection Dry

  • Drug Facts

    Active ingredient
    Aluminum Chlorohydrate (23.3%)

  • Purpose

    antiperspirant

  • Uses

    reduces underarm wetness

  • 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°F/50°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

    • KEEP OUT OF REACH OF CHILDREN.

  • Directions

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

  • Inactive ingredients

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

  • Questions?

    Call toll-free 1-800-450-7580

  • Packaging

    AxePhoenixDrySprayAP

  • INGREDIENTS AND APPEARANCE
    AXE 
    phoenix dry spray antiperspirant 48hr protection dry aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1570
    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)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    PROPANE (UNII: T75W9911L6)  
    ISOBUTANE (UNII: BXR49TP611)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1570-1107 g in 1 CAN; Type 0: Not a Combination Product02/03/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35002/03/2018
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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