Label: DOVE- clinical protection original clean antiperspirant and deodorant stick

  • NDC Code(s): 64942-2269-1, 64942-2269-2
  • Packager: Conopco Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 8, 2024

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  • DOVE CLINICAL PROTECTION ORIGINAL CLEAN ANTIPERSPIRANT & DEODORANT - aluminum zirconium tetrachlorohydrex gly stick

  • Drug Facts

    Active ingredient

    Aluminum Zirconium Tetrachlorohydrex GLY (20.0 %)

  • Purpose

    antiperspirant

  • Uses

    • reduces underarm wetness
    • extra effective

  • 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

    • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • apply to underarms only
    • before bed, apply two clicks of product to each underarm

  • Other information

    Do not store over 115°F

  • Inactive ingredients

    Cyclopentasiloxane, Dimethicone, Microcrystalline Wax, Paraffin, Fragrance (Parfum), Silica, Dimethicone Crosspolymer, Helianthus Annuus (Sunflower) Seed Oil, BHT, Benzyl Alcohol, Benzyl Salicylate, Cinnamyl Alcohol, Citronellol, Eugenol, Geraniol, Hexyl Cinnamal, Isoeugenol, Linalool

  • Questions?

    Call toll-free 1-800-761-3683

  • Packaging

    Dove Original Clean AP IS Carton

  • INGREDIENTS AND APPEARANCE
    DOVE 
    clinical protection original clean antiperspirant and deodorant stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2269
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    EUGENOL (UNII: 3T8H1794QW)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
    CINNAMYL ALCOHOL (UNII: SS8YOP444F)  
    GERANIOL (UNII: L837108USY)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    ISOEUGENOL (UNII: 5M0MWY797U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2269-21 in 1 CARTON04/14/2023
    1NDC:64942-2269-148 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01904/14/2023
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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