Label: DR. GROOT ANTI-DANDRUFF SCALP CARE 2 IN 1- salicylic acid shampoo
- NDC Code(s): 53208-902-36
- Packager: LG H&H CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 31, 2024
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Inactive Ingredients
water, sodium C14-16 olefin sulfonate, cocamidopropyl betaine, disodium cocoyl glutamate, sodium chloride, PEG-7 glyceryl cocoate, polyquaternium-7, fragrance, sodium cocoyl glutamate, sodium benzoate, PEG-40 hydrogenated castor oil, menthol, tetrasodium EDTA, citric acid, biotin, caffeine, hexylene glycol, honey, niacinamide, panthenol, sodium citrate, polysorbate 20, alcohol, butylene glycol, propolis extract, houttuynia cordata extract, rosmarinus officinalis (rosemary) leaf extract, zingiber officinale (ginger) root extract
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- PRINCIPAL DISPLAY PANEL - 300 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
DR. GROOT ANTI-DANDRUFF SCALP CARE 2 IN 1
salicylic acid shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-902 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength CAFFEINE (UNII: 3G6A5W338E) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PANTHENOL (UNII: WV9CM0O67Z) POLYSORBATE 20 (UNII: 7T1F30V5YH) ALCOHOL (UNII: 3K9958V90M) HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM CHLORIDE (UNII: 451W47IQ8X) DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) HONEY (UNII: Y9H1V576FH) NIACINAMIDE (UNII: 25X51I8RD4) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) SODIUM BENZOATE (UNII: OJ245FE5EU) BIOTIN (UNII: 6SO6U10H04) ROSEMARY (UNII: IJ67X351P9) GINGER (UNII: C5529G5JPQ) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) MENTHOL (UNII: L7T10EIP3A) PROPOLIS WAX (UNII: 6Y8XYV2NOF) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53208-902-36 300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/31/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 05/31/2024 Labeler - LG H&H CO., LTD. (688276187) Establishment Name Address ID/FEI Business Operations TAI GUK PHARM. CO., LTD 689060246 manufacture(53208-902)

