Label: CERAVE DEVELOPED WITH DERMATOLOGISTS ECZEMA RELIEF CREAMY- oatmeal oil

  • NDC Code(s): 49967-951-01, 49967-951-02
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2024

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  • Active ingredient

    Colloidal oatmeal 1%

  • Purpose

    Skin protectant

  • Uses

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

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    apply as needed

  • Inactive ingredients

    water, cetearyl alcohol, glycerin, cetyl alcohol, ceteareth-20, olea europaea (olive) fruit oil, isononyl isononanoate, carthamus tinctorius (safflower) seed oil, PEG-100 stearate, potassium phosphate, allantoin, ceramide NP, ceramide AP, ceramide EOP, carbomer, niacinamide, glyceryl stearate. glycine soja (soybean) oil, behentrimonium methosulfate, vitis vinifera (grape) seed oil, sodium PCA, ophiopogon japonicus root extract, sodium lauroyl lactylate, helianthus annuus (sunflower) seed oil, cholesterol, rosmarinus officinalis (rosemary) extract, rosmarinus officinalis (rosemary) leaf extract, phenoxyethanol, chlorphenesin, dipotassium phosphate, tocopherol, propylheptyl caprylate, hydroxyacetophenone, hydrolyzed hyaluronic acid, persea gratissima (avocado) oil, xanthan gum, phytosphingosine, ethylhexylglycerin

  • Questions or comments?

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  • PRINCIPAL DISPLAY PANEL

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  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    CERAVE DEVELOPED WITH DERMATOLOGISTS ECZEMA RELIEF CREAMY 
    oatmeal oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-951
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    MONOBASIC POTASSIUM PHOSPHATE (UNII: 4J9FJ0HL51)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CERAMIDE NP (UNII: 4370DF050B)  
    CERAMIDE AP (UNII: F1X8L2B00J)  
    CERAMIDE 1 (UNII: 5THT33P7X7)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)  
    GRAPE SEED OIL (UNII: 930MLC8XGG)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    OPHIOPOGON JAPONICUS ROOT (UNII: 90PS6JV9GZ)  
    SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    ROSEMARY (UNII: IJ67X351P9)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    AVOCADO OIL (UNII: 6VNO72PFC1)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-951-01236 mL in 1 TUBE; Type 0: Not a Combination Product12/01/2020
    2NDC:49967-951-02100 mL in 1 TUBE; Type 0: Not a Combination Product12/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/01/2020
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'OREAL USA PRODUCTS, INC.624244349manufacture(49967-951)
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