Label: SATINIQUE ANTI DANDRUFF SCALP AND HAIR- salicylic acid liquid
- NDC Code(s): 10056-536-00, 10056-536-01
- Packager: Access Business Group LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 9, 2024
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- Active Ingredients
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Inactive ingredients:
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Cocamidopropyl Hydroxysultaine, Sodium Chloride, Cetyl Alcohol, Acrylates Copolymer, Fragrance, Glycerin, Sodium Benzoate, Sodium Lauroyl Sarcosinate, Benzyl Alcohol, Sodium Hydroxide, Guar Hydroxypropyltrimonium Chloride, Polystyrene, Caprylic/-Capric Triglyceride, Lauric Acid, Tetrasodium EDTA, Polyquaternium-39, Creatine, Xanthan Gum, Ethylhexyglycerin, Phenoxyethanol, Butylene Glycol, Glycereth- 26, C11-15 Pareth-40, Tocopherol, Lecithin, C11-15 Alketh-7, Zingiber Officinale (Ginger) Root Extract, Helianthus Annuus (Sunflower) Seed Oil, Chenopodium Quinoa Seed Extract, Argania Spinosa Kernel Oil, Poloxamer 331, Hydrolyzed Adansonia Digitata Seed Extract, Myristic Acid, PPG-12-Buteth-16, Sodium Hyaluronate, Ceramide NP, Propylene Glycol, Phytosphingosine, Beta- Sitosterol, Chlorphenesin, Hydrogenated Lecithin, Potassium Sorbate, Citronellol, Geraniol, Hexyl Cinnamal, Limonene, Linalool
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INGREDIENTS AND APPEARANCE
SATINIQUE ANTI DANDRUFF SCALP AND HAIR
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10056-536 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 C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) SODIUM CHLORIDE (UNII: 451W47IQ8X) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERIN (UNII: PDC6A3C0OX) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) BENZYL ALCOHOL (UNII: LKG8494WBH) SODIUM HYDROXIDE (UNII: 55X04QC32I) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) LAURIC ACID (UNII: 1160N9NU9U) EDETATE SODIUM (UNII: MP1J8420LU) CREATINE (UNII: MU72812GK0) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERETH-26 (UNII: NNE56F2N14) C11-15 PARETH-40 (UNII: L774F88277) TOCOPHEROL (UNII: R0ZB2556P8) C11-15 ALKETH-7 (UNII: 261HPE0IS3) GINGER (UNII: C5529G5JPQ) SUNFLOWER OIL (UNII: 3W1JG795YI) CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X) ARGAN OIL (UNII: 4V59G5UW9X) POLOXAMER 331 (UNII: IS93EQR73R) MYRISTIC ACID (UNII: 0I3V7S25AW) PPG-12-BUTETH-16 (UNII: 58CG7042J1) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CERAMIDE NP (UNII: 4370DF050B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) .BETA.-SITOSTEROL (UNII: S347WMO6M4) CHLORPHENESIN (UNII: I670DAL4SZ) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) GERANIOL (UNII: L837108USY) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+/-)- (UNII: D81QY6I88E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10056-536-00 280 mL in 1 CONTAINER; Type 0: Not a Combination Product 02/01/2025 2 NDC:10056-536-01 750 mL in 1 CONTAINER; Type 0: Not a Combination Product 02/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 02/01/2025 Labeler - Access Business Group LLC (839830713)
