Label: LA ROCHE POSAY EFFACLAR MEDICATED CLEANSER- salicylic acid gel
- NDC Code(s): 49967-402-01, 49967-402-02, 49967-402-03
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 2, 2024
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- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, sodium laureth sulfate, decyl glucoside, glycerin, sodium chloride, coco-betaine, sodium hydroxide, PEG-150 pentaerythrityl tetrastearate, citric acid, hexylene glycol, PEG-6 caprylic/capric glycerides, zinc gluconate, tetrasodium EDTA, polyquaternium-47, menthol, capryloyl salicylic acid, sodium benzoate
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INGREDIENTS AND APPEARANCE
LA ROCHE POSAY EFFACLAR MEDICATED CLEANSER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-402 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 LAURETH SULFATE (UNII: BPV390UAP0) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) COCO-BETAINE (UNII: 03DH2IZ3FY) SODIUM HYDROXIDE (UNII: 55X04QC32I) PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8) ZINC GLUCONATE (UNII: U6WSN5SQ1Z) EDETATE SODIUM (UNII: MP1J8420LU) POLYQUATERNIUM-47 (METHACRYLAMIDOPROPYLTRIMETHYLAMMONIUM CHLORIDE-CO-METHYL ACRYLATE-CO-ACRYLIC ACID 46:8:46; 1300000 MW) (UNII: G938900MID) MENTHOL (UNII: L7T10EIP3A) CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-402-01 200 mL in 1 TUBE; Type 0: Not a Combination Product 08/01/2022 2 NDC:49967-402-02 100 mL in 1 TUBE; Type 0: Not a Combination Product 08/01/2022 3 NDC:49967-402-03 15 mL in 1 TUBE; Type 0: Not a Combination Product 08/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/01/2022 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 manufacture(49967-402) , pack(49967-402)