Label: DOVE DERMASERIES ECZEMA THERAPY CREAM- oatmeal cream

  • NDC Code(s): 64942-1306-1, 64942-1306-2, 64942-1306-3
  • 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 5, 2022

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

  • ACTIVE INGREDIENT

    Active ingredient

    Colloidal Oatmeal (1.0%)

  • PURPOSE

    Purpose

    Skin protectant

  • INDICATIONS & USAGE

    Uses

    Temporarily protects and helps relieve minor skin irritation and itching due to: ● eczema  rashes

  • WARNINGS

    WARNINGS
    For External Use Only.

    When using this product do not get into eyes.

    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

    Do not use on

    deep or puncture wounds

    animal bites

    serious burns

    Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions

    ● apply as needed.

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Water (Aqua), Glycerin, Dimethicone, Hydroxystearic Acid, Sodium Hydroxypropyl Starch Phosphate, Isopropyl Myristate, Petrolatum, Cetearyl Alcohol, Glyceryl Hydroxystearate, Caprylyl Glycol, Phenoxyethanol, Stearic Acid, Citrus Limon (Lemon) Peel Powder, Cetearyl Glucoside, Citrus Aurantifolia (Lime) Peel Powder, Disodium EDTA, Titanium Dioxide (CI 77891).

  • QUESTIONS

    Questions or comments?

    Call 1-800-761-DOVE (3683)

  • 4.1 FL. OZ. PDP

    DoveDermaSeriesEczemaTherapyCream

  • 4.1 Fl. OZ. Carton

    DoveDermaSeriesEczemaTherapyCream

  • INGREDIENTS AND APPEARANCE
    DOVE DERMASERIES  ECZEMA THERAPY CREAM
    oatmeal cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1306
    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)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    LEMON PEEL (UNII: 72O054U628)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    LIME PEEL (UNII: 544EQK5Q0W)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1306-21 in 1 CARTON10/15/2013
    1NDC:64942-1306-1120 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:64942-1306-315 mL in 1 TUBE; Type 0: Not a Combination Product10/15/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34710/15/2013
    Labeler - Conopco Inc. d/b/a Unilever (001375088)
    Registrant - Conopco Inc. d/b/a Unilever (001375088)