Label: DOVE- care and protect antibacterial beauty bar soap

  • NDC Code(s): 64942-1845-1, 64942-1845-2, 64942-1845-3, 64942-1845-4, view more
    64942-1845-5, 64942-1845-6
  • Packager: Conopco Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 17, 2024

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  • DOVE CARE & PROTECT ANTIBACTERIAL BEAUTY BAR - Benzalkonium Chloride soap

    Dove Care & Protect Antibacterial Beauty Bar

  • 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

    Wet bar with water, lather vigorously and use all over body. Rinse clean.

  • Inactive ingredients

    Sodium Lauroyl Isethionate, Stearic Acid, Sodium Oleate, Sodium Stearate, Water (Aqua), Sodium Isethionate, Lauric Acid, Sodium C14-16 Olefin Sulfonate, Sodium Laurate, Fragrance (Parfum), Dipropylene Glycol, Sodium Chloride, Tetrasodium Etidronate, Tetrasodium EDTA, Kaolin*, Titanium Dioxide*, Blue 1 (CI 42090), Yellow 5 (CI 19140). *Contains one or more of these ingredients

  • Questions or Comments?

    1-800-761-3683

  • Packaging

    Dove Antibacterial Beauty Bar

  • INGREDIENTS AND APPEARANCE
    DOVE 
    care and protect antibacterial beauty bar soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1845
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SODIUM LAUROYL ISETHIONATE (UNII: M590021Z02)  
    SODIUM OLEATE (UNII: 399SL044HN)  
    SODIUM STEARATE (UNII: QU7E2XA9TG)  
    SODIUM ISETHIONATE (UNII: 3R36J71C17)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    SODIUM LAURATE (UNII: K146MR5EXO)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)  
    KAOLIN (UNII: 24H4NWX5CO)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1845-1270 g in 1 CARTON; Type 0: Not a Combination Product01/15/2021
    2NDC:64942-1845-2425 g in 1 CARTON; Type 0: Not a Combination Product01/15/2021
    3NDC:64942-1845-3636 g in 1 CARTON; Type 0: Not a Combination Product01/15/2021
    4NDC:64942-1845-4212 g in 1 CARTON; Type 0: Not a Combination Product01/15/2021
    5NDC:64942-1845-5600 g in 1 CARTON; Type 0: Not a Combination Product01/15/2021
    6NDC:64942-1845-6425 g in 1 CARTON; Type 0: Not a Combination Product01/15/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01601/15/2021
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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