Label: DOVE- men plus care eucalyptus plus birch dry spray 48h antiperspirant aerosol, spray

  • NDC Code(s): 64942-2321-1
  • Packager: Conopco, Inc. d/b/a Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 24, 2024

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  • DOVE MEN + CARE EUCALYPTUS + BIRCH DRY SPRAY 48H ANTIPERSPIRANT - aluminum chlorohydrate aerosol, spray

  • Drug Facts

    Active ingredient

    Aluminum Chlorohydrate (20.2%)

  • Purpose

    antiperspirant

  • Uses



    reduces underarm wetness

  • Warnings

    • 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

  • Inactive ingredients

    Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Disteardimonium Hectorite, C12-15 Alkyl Benzoate, Propane, BHT, Octyldodecanol, Propylene Carbonate, Dimethiconol, Benzyl Alcohol, Benzyl Salicylate, Citronellol, Coumarin, Geraniol, Limonene, Linalool

  • Questions?


    Call toll-free 1-800-761-3683

  • Packaging

    Dove Men Eucalyptus Dry Spray AP

  • INGREDIENTS AND APPEARANCE
    DOVE 
    men plus care eucalyptus plus birch dry spray 48h antiperspirant aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2321
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    BUTANE (UNII: 6LV4FOR43R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ISOBUTANE (UNII: BXR49TP611)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    PROPANE (UNII: T75W9911L6)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    DIMETHICONOL (40 CST) (UNII: 343C7U75XW)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    COUMARIN (UNII: A4VZ22K1WT)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    GERANIOL (UNII: L837108USY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2321-1107 g in 1 CAN; Type 0: Not a Combination Product06/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01906/24/2024
    Labeler - Conopco, Inc. d/b/a Unilever (001375088)
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