Label: DOVE- hand sanitizer shea butter gel

  • NDC Code(s): 64942-1746-1, 64942-1746-2, 64942-1746-3
  • 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 April 29, 2022

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  • DOVE NOURISHING HAND SANITIZER SHEA BUTTER & WARM VANILLA 8H MOISTURIZATION - Ethyl Alcohol gel

    Dove Nourishing Hand Sanitizer Shea Butter & Warm Vanilla 8h Moisturization

  • Drug Facts

    Active ingredient

    Ethyl Alcohol 61%

  • Purpose

    Antiseptic

  • Uses

    • Hand sanitizer to help reduce bacteria on the skin

  • Warnings

    • For external use only
    • Flammable. Keep away from fire or flame
    • Avoid contact with eyes,     in case of contact, rinse eyes thoroughly with water immediately.
    • If irritation develps, discontinue use and consult a doctor.

  • 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

  • Other information

    • Store below 105˚F (40˚C).
    • May discolor fabrics or surfaces.

  • Inactive ingredients

    Water (Aqua), Glycerin, Butylene Glycol, Dimethicone, Glycine Soja (Soybean) Oil, Fragrance (Parfum), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Echium Plantagineum Seed Oil, Aminomethyl Propanol, Hydrogenated Lecithin, Tocopherol, Xanthan Gum, Stearic Acid, Citric Acid, Benzyl Alcohol, Coumarin, Hexyl Cinnamal, Limonene, Linalool .

  • Questions?

    1-800-761-3683

  • Packaging

    DoveHandSanitizerSheaButter

  • INGREDIENTS AND APPEARANCE
    DOVE 
    hand sanitizer shea butter gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1746
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL610 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    COUMARIN (UNII: A4VZ22K1WT)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1746-1236 mL in 1 CONTAINER; Type 0: Not a Combination Product07/21/2020
    2NDC:64942-1746-259 mL in 1 CONTAINER; Type 0: Not a Combination Product07/21/2020
    3NDC:64942-1746-31000 mL in 1 CONTAINER; Type 0: Not a Combination Product07/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/21/2020
    Labeler - Conopco Inc. d/b/a/ Unilever (001375088)
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