Label: BABY DOVE- eczema care soothing cream cream

  • NDC Code(s): 64942-1873-1
  • Packager: Conopco, Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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.

  • Description

    BABY DOVE ECZEMA CARE SOOTHING CREAM - (colloidal oatmeal) cream

  • Drug Facts

    Active ingredient
    Colloidal Oatmeal (1%)

  • Purpose

    Skin Protectant

  • Uses

    temporarily protects and helps relieve minor skin irritation and itching due to:

    • eczema

  • Warnings

    For external use only
    When using this product
    do not get into eyes.r.
    Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Apply as needed

  • Other Information

    Do not use if tamper evident seal is missing or broken.

  • Inactive ingredients

    Water (Eau), Glycerin, Dimethicone, Butyrospermum Parkii (Shea) Butter, Copernicia Cerifera (Carnauba) Wax, Isopropyl Myristate, Cetearyl Alcohol, Glyceryl Hydroxystearate, Dimethicone Crosspolymer, Hydroxystearic Acid, Caprylyl Glycol, Cetearyl Glucoside, Sodium Cetearyl Sulfate, Cetyl Palmitate, Sodium Benzoate, Phenoxyethanol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Stearic Acid, Tetrasodium EDTA.

  • Questions or comments?

    1-800-761-3683

  • Packaging

    Baby Dove Eczema Cream BackBaby Dove Eczema Cream Front

  • INGREDIENTS AND APPEARANCE
    BABY DOVE 
    eczema care soothing cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1873
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GLYCERYL HYDROXYSTEARATE (UNII: UJ6CAW9YNV)  
    DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
    12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
    CETYL PALMITATE (UNII: 5ZA2S6B08X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1873-1144 mL in 1 TUBE; Type 0: Not a Combination Product03/05/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34703/05/2021
    Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)