Label: CERAVE DEVELOPED WITH DERMATOLOGIST BABY ECZEMA RELIEF CREAM- oatmeal cream
- NDC Code(s): 49967-536-01
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 28, 2025
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- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, butyrospermum parkii (shea) butter, glycerin, dimethicone, cetearyl alcohol, niacinamide, caprylic/capric triglyceride, glyceryl stearate, PEG-100 stearate, ammonium polyacryloyldimethyl taurate, ceramide np, ceramide ap, ceramide eop, sorbitan tristearate, carbomer, cetearyl isononanoate, behentrimonium methosulfate, triethyl citrate, sodium benzoate, sodium lauroyl lactylate, sodium hyaluronate, cholesterol, phenoxyethanol, tocopherol, citric acid, caprylyl glycol, trisodium ethylenediamine disuccinate, xanthan gum, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, phytosphingosine, octyldodecanol, benzoic acid, PEG-20 methyl glucose sesquistearate
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INGREDIENTS AND APPEARANCE
CERAVE DEVELOPED WITH DERMATOLOGIST BABY ECZEMA RELIEF CREAM
oatmeal creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-536 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OATMEAL (UNII: 8PI54V663Y) (OATMEAL - UNII:8PI54V663Y) OATMEAL 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) CETEARYL ALCOHOL (UNII: 2DMT128M1S) NIACINAMIDE (UNII: 25X51I8RD4) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) GLYCERYL STEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: F01RIY4371) CERAMIDE NP (UNII: 4370DF050B) CERAMIDE AP (UNII: F1X8L2B00J) SORBITAN TRISTEARATE (UNII: 6LUM696811) CARBOMER (UNII: 0A5MM307FC) CETEARYL ISONONANOATE (UNII: P5O01U99NI) BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) SODIUM HYALURONATE (UNII: YSE9PPT4TH) CHOLESTEROL (UNII: 97C5T2UQ7J) PHENOXYETHANOL (UNII: HIE492ZZ3T) TOCOPHEROL (UNII: R0ZB2556P8) CITRIC ACID (UNII: 2968PHW8QP) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) XANTHAN GUM (UNII: TTV12P4NEE) PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) OCTYLDODECANOL (UNII: 461N1O614Y) BENZOIC ACID (UNII: 8SKN0B0MIM) PEG-20 METHYL GLUCOSE SESQUISTEARATE (UNII: 0345752X7U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-536-01 148 mL in 1 TUBE; Type 0: Not a Combination Product 01/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 01/01/2025 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA PRODUCTS, INC. 624244349 manufacture(49967-536)