Label: CERAVE DEVELOPED WITH DERMATOLOGISTS BABY MOISTURIZING- dimethicone lotion
- NDC Code(s): 49967-190-01, 49967-190-02
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 29, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use on
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
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Inactive ingredients
purified water, caprylic/capric triglyceride, cetostearyl alcohol, cetyl alcohol, emulsifying wax, phenoxyethanol,niacinamide, ceramide 3, ceramide 6-II, ceramide 1, hyaluronic acid, allantoin, tocopheryl acetate, lauric acid, zinc citrate, polyglyceryl-3 diisostearate, bBehentrimonium methosulfate, sodium lauroyl lactylate, arginine PCA, potassium phosphate, dipotassium phosphate, EDTA, sodium PCA, phytosphingosine, cholesterol, xanthan gum, carbomer, ethylhexylglycerin
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INGREDIENTS AND APPEARANCE
CERAVE DEVELOPED WITH DERMATOLOGISTS BABY MOISTURIZING
dimethicone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-190 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ALCOHOL (UNII: 936JST6JCN) PHENOXYETHANOL (UNII: HIE492ZZ3T) NIACINAMIDE (UNII: 25X51I8RD4) CERAMIDE 3 (UNII: 4370DF050B) CERAMIDE 6 II (UNII: F1X8L2B00J) HYALURONIC ACID (UNII: S270N0TRQY) ALLANTOIN (UNII: 344S277G0Z) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) LAURIC ACID (UNII: 1160N9NU9U) ZINC CITRATE (UNII: K72I3DEX9B) POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8) BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) EDETIC ACID (UNII: 9G34HU7RV0) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) CHOLESTEROL (UNII: 97C5T2UQ7J) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-190-01 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/17/2017 05/31/2024 2 NDC:49967-190-02 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/17/2017 05/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 08/17/2017 05/31/2024 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA Products, Inc. 624244349 MANUFACTURE(49967-190)