Label: DOVE- care and protect antibacterial hand wash liquid

  • NDC Code(s): 64942-1847-1
  • 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 December 7, 2022

If you are a consumer or patient please visit this version.

  • 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 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

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

  • Inactive ingredients

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

  • 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:64942-1847
    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
    PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)  
    SODIUM LAUROYL GLYCINATE (UNII: L54QIO80PN)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM LAUROYL ISETHIONATE (UNII: M590021Z02)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1847-1400 mL in 1 BOTTLE, PUMP; 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)