Label: DOVE- advanced care beauty finish dry spray 72h antiperspirant deodorant aerosol, spray

  • NDC Code(s): 64942-2234-1, 64942-2234-2
  • Packager: Conopco, Inc. d/b/a Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 20, 2023

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  • DOVE ADVANCED CARE BEAUTY FINISH DRY SPRAY 72H ANTIPERSPIRANT DEODORANT - aluminum sesquichlorohydrate aerosol, spray

  • Drug Facts

    Active ingredient

    Aluminum Sesquichlorohydrate (15.2)

  • 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, Glycine, Helianthus Annuus (Sunflower) Seed Oil, Fragrance (Parfum), C12-15 Alkyl Benzoate, Disteardimonium Hectorite, Calcium Chloride, Propane, BHT, Octyldodecanol, Propylene Carbonate, Dimethiconol, Benzyl Alcohol, Benzyl Benzoate, Citronellol, Geraniol, Hexyl Cinnamal, Limonene, Linalool

  • Questions?


    Call toll-free 1-800-761-3683

  • Packaging

    Dove Beauty Finish Dry Spray AP

  • INGREDIENTS AND APPEARANCE
    DOVE 
    advanced care beauty finish dry spray 72h antiperspirant deodorant aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2234
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE15.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL BENZOATE (UNII: N863NB338G)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    DIMETHICONOL (40 CST) (UNII: 343C7U75XW)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    GLYCINE (UNII: TE7660XO1C)  
    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)  
    GERANIOL (UNII: L837108USY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2234-1107 g in 1 CAN; Type 0: Not a Combination Product11/01/2023
    2NDC:64942-2234-270 g in 1 CAN; Type 0: Not a Combination Product11/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02611/01/2023
    Labeler - Conopco, Inc. d/b/a Unilever (001375088)
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