Label: CERAVE DEVELOPED WITH DERMATOLOGISTS ACNE CONTROL CLEANSER OIL ABSORBING TECHNOLOGY- salicylic acid gel
- NDC Code(s): 49967-840-01, 49967-840-02
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 28, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, cocamidopropyl hydroxysultaine, glycerin, sodium lauroyl sarcosinate, niacinamide, sodium methyl cocoyl taurate, PEG-150 pentaerythrityl tetrastearate, gluconolactone, sodium cocoyl isethionate, ceramide NP, ceramide AP, ceramide EOP, carbomer, calcium gluconate, triethyl citrate, sodium hydroxide, sodium benzoate, sodium chloride, sodium lauroyl lactylate, cholesterol, coconut acid, tetrasodium EDTA, caprylyl glycol, hydrolyzed hyaluronic acid, trisodium ethylenediamine disuccinate, hectorite, phytosphingosine, xanthan gum, acrylates copolymer, benzoic acid
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INGREDIENTS AND APPEARANCE
CERAVE DEVELOPED WITH DERMATOLOGISTS ACNE CONTROL CLEANSER OIL ABSORBING TECHNOLOGY
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-840 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) GLYCERIN (UNII: PDC6A3C0OX) NIACINAMIDE (UNII: 25X51I8RD4) GLUCONOLACTONE (UNII: WQ29KQ9POT) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM HYDROXIDE (UNII: 55X04QC32I) HECTORITE (UNII: 08X4KI73EZ) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO) CHOLESTEROL (UNII: 97C5T2UQ7J) COCONUT ACID (UNII: 40U37V505D) EDETATE SODIUM (UNII: MP1J8420LU) CALCIUM GLUCONATE (UNII: SQE6VB453K) CERAMIDE NP (UNII: 4370DF050B) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CERAMIDE AP (UNII: F1X8L2B00J) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) HYALURONIC ACID (UNII: S270N0TRQY) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) BENZOIC ACID (UNII: 8SKN0B0MIM) CERAMIDE 1 (UNII: 5THT33P7X7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-840-01 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2023 2 NDC:49967-840-02 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 03/31/2023 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA, INC. 960317444 manufacture(49967-840) , pack(49967-840) Establishment Name Address ID/FEI Business Operations L'Oreal USA Products, Inc. 624244349 manufacture(49967-840) , pack(49967-840)