Label: DOVE- care and protect antibactercial body wash liquid

  • NDC Code(s): 64942-2121-1, 64942-2121-2
  • 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 May 24, 2023

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  • DOVE CARE & PROTECT ANTIBACTERCIAL BODY WASH - benzalkonium chloride liquid

  • 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 Chloride, Cocamidopropyl Betaine, Sodium Lauroyl Isethionate, Acrylates Copolymer, Lauric Acid, Glycerin, Fragrance (Parfum), Phenoxyethanol, Glycol Distearate, Stearic Acid, Palmitic Acid, Tetrasodium EDTA, PEG-150 Pentaerythrityl Tetrastearate, PPG-2 Hydroxyethyl Cocamide, Helianthus Annuus (Sunflower) Seed Oil, Iodopropynyl Butylcarbamate, Citric Acid, Sodium Benzoate, Geraniol, Limonene, Linalool.

  • Questions or comments?

    1-800-761-3683

  • PRINCIPAL DISPLAY PANEL

    Dove Antibactercial Body Wash

  • INGREDIENTS AND APPEARANCE
    DOVE 
    care and protect antibactercial body wash liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2121
    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
    PALMITIC ACID (UNII: 2V16EO95H1)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    GERANIOL (UNII: L837108USY)  
    SODIUM LAUROYL ISETHIONATE (UNII: M590021Z02)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2121-1591 mL in 1 BOTTLE; Type 0: Not a Combination Product05/24/2023
    2NDC:64942-2121-2905 mL in 1 BOTTLE; Type 0: Not a Combination Product05/24/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/24/2023
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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