Label: DOVE- men plus care antibactercial skin defense body and face wash liquid

  • NDC Code(s): 64942-2107-1, 64942-2107-2, 64942-2107-3
  • Packager: Conopco Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 November 11, 2022

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  • DOVE MEN + CARE ANTIBACTERCIAL SKIN DEFENSE BODY + FACE WASH - benzalkonium chloride liquid

    Dove Men+Care Antibactercial Skin Defense Body + Face Wash

  • Drug Facts

    Active ingredient

    Benzalkonium Chloride (0.13%)

  • Purpose

    Antibacterial

  • Uses

    For washing to decrease bacteria on the skin

  • Warnings

    • For external use only
    • When using this product     do not use in or near the eyes. In case of contact, rinse eyes thoroughly with wate r
    • Stop use and ask doctor     if irritation or redness develop.

  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children except under adult supervision.

    If swallowed, get medical help or contact a poison control Center right away.

  • Directions

    Dispense into hands, wash cloth or pouf, work into lather and use all over body. Rinse clean.

  • Inactive ingredients

    Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Glycerin, Fragrance (Parfum), Stearic Acid, Palmitic Acid, Sodium Chloride, Sodium Benzoate, Citric Acid, Tetrasodium EDTA, PPG-9, Limonene, Linalool, Yellow 5, Red 33

  • Questions?

    1-800-761-3683

  • Packaging

    Dove Men Skin Defense Wash

  • INGREDIENTS AND APPEARANCE
    DOVE 
    men plus care antibactercial skin defense body and face wash liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2107
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PPG-9 (UNII: I29VQH0G0B)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2107-1532 mL in 1 BOTTLE; Type 0: Not a Combination Product01/16/2023
    2NDC:64942-2107-2400 mL in 1 BOTTLE; Type 0: Not a Combination Product01/16/2023
    3NDC:64942-2107-3887 mL in 1 BOTTLE; Type 0: Not a Combination Product01/16/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/16/2023
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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