Label: DOVE DERMASERIES ECZEMA RELIEF SOOTHING BODY- colloidal oatmeal lotion

  • NDC Code(s): 64942-1503-1, 64942-1503-2
  • Packager: Conopco, Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 24, 2024

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

View All Sections
  • Drug Facts

  • Active ingredients

    Colloidal Oatmeal 1.0%

  • Purpose

    Skin Protectant

  • Uses

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

  • 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.

  • 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
    • Massage into extremely dry, cracked and chafed skin as often as needed for instant relief and long-lasting hydration
    • Apply generously onto dry skin and problem areas twice daily
  • Inactive ingredients

    Water (Aqua), Glycerin, Stearic Acid, Isopropyl Palmitate, Glycol Stearate, PEG-100 Stearate, Mineral Oil, Dimethicone, Glyceryl Stearate, Petrolatum, Cetyl Alcohol, Phenoxyethanol, Methylparaben, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Propylparaben, Stearamide AMP, Disodium EDTA, Silk Amino Acids, Ascorbic Acid, Panthenol, Tocopheryl Acetate, Biotin, Niacinamide. 

  • Questions or comments?

    1-800-761-3683

  • SPL UNCLASSIFIED SECTION

    Clinically tested to soothe dry, itchy, irritated skin tested with dermatologists

    Fragrance free • steroid free

  • Packaging

    Dovelotion1503

  • INGREDIENTS AND APPEARANCE
    DOVE  DERMASERIES ECZEMA RELIEF SOOTHING BODY
    colloidal oatmeal lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1503
    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
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    STEARAMIDE AMP (UNII: U3K8640346)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    AMINO ACIDS, SILK (UNII: V0L00EX1IA)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    BIOTIN (UNII: 6SO6U10H04)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1503-150 mL in 1 TUBE; Type 0: Not a Combination Product07/13/2017
    2NDC:64942-1503-2200 mL in 1 TUBE; Type 0: Not a Combination Product07/13/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01607/13/2017
    Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!