Label: DOVE- care and protect antibacterial hand wash liquid

  • NDC Code(s): 64942-2105-1, 64942-2105-2
  • 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 November 10, 2022

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  • DOVE CARE & PROTECT ANTIBACTERIAL HAND WASH - Benzalkonium Chloride

    Dove Care & Protect Antibacterial Hand 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 thoroyghly with water.
    • Stop use and ask doctor if irritation or redness develop

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

  • 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

    Pump into wet hands and lather vigorously. Rinse and dry thoroughtly

  • Inactive ingredients

    Water, Sodium Methyl Lauroyl Taurate, Glycerin, Sodium Hydroxypropyl Starch Phosphate, Citric Acid, Sodium Benzoate, Cocamidopropyl Betaine, Fragrance (Parfum), Lauric Acid, Stearic Acid, Palmitic Acid, Hydroxystearic Acid, Glyceryl Stearate, Guar Hydroxypropyltrimonium Chloride, Microcrystalline Cellulose, Sodium Gluconate, Cellulose Gum, Benzyl Alcohol, Limonene.

  • Questions or Comments?

    1-800-761-3683

  • Packaging

    Dove Antibacterial Hand Wash

  • INGREDIENTS AND APPEARANCE
    DOVE 
    care and protect antibacterial hand wash liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2105
    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
    SODIUM LAUROYL METHYL TAURATE (UNII: H5K9S87SP3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2105-1355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2023
    2NDC:64942-2105-21000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2023
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
    Establishment
    NameAddressID/FEIBusiness Operations
    CONOPCO Inc. d/b/a Unilever043510056manufacture(64942-2105)
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