Label: DOVE- dove men plus care skin defense body wash liquid

  • NDC Code(s): 64942-1836-1, 64942-1836-2, 64942-1836-3
  • Packager: Conopco Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL

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 7, 2022

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  • DOVE MEN +CARE SKIN DEFENSE BODY WASH - Benzalkonium Chloride

    Dove Men +Care Skin Defense Body 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 (Aqua), Sodium C12-13 Pareth Sulfate, Cocamidopropyl Betaine, Glycerin, Sodium Chloride, Fragrance (Parfum), Stearic Acid, Palmitic Acid, Citric Acid, Sodium Benzoate, Tetrasodium EDTA, PPG-9, Limonene, Linalool, Red 33 (CI 17200), Yellow 5 (CI 19140).

  • Questions?

    Call toll-free 1-800-761-3683

  • Packaging

    Dove Men Skin Defense Body Wash

  • INGREDIENTS AND APPEARANCE
    DOVE 
    dove men plus care skin defense body wash liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1836
    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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1836-1532 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2021
    2NDC:64942-1836-2400 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2021
    3NDC:64942-1836-3887 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/15/2021
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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