Label: SATINIQUE ANTI DANDRUFF- pyrithione zinc cream
- NDC Code(s): 10056-006-01
- Packager: Access Business Group LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 23, 2023
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- Drug Facts
- Active Ingredients
- Uses
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Inactive Ingredients
Water, Sodium Laureth Sulfate, Decyl Glucoside, Glycol Distearate, Disodium Laureth Sulfosuccinate, Glycereth-26, Ceramide 2 , Ceramide-3, C10-40 isoalkylamidopropylethyldimonium ethosulfate, Creatine, Fragrance, Dimethicome, Sodium Chloride, C12-15 Alkyl Lactate, Hydroxypropyl Methylcellulose, Guar Hydroxypropyltrimonium Chloride, Zinc Chloride, Hectorite, Hydroxyethylcellulose, Tetrasodium EDTA, Citric Acid, Tocopheryl Acetate, Limnanthes Alba (Meadowfoam) Seed Oil, Propylene Glycol, Aloe Barbadensis Leaf Juice, Butyl Avodate, PPG-12-Buteth-15, Triethanolamine, Sodium PCA, Sodium Lactate, Arginine, Aspartic Acid, PCA, Glycine, Alanine, MethylChlororisothiazolinone, Serine, Valine, Behenic Acid, Cholesterol, Isoleucine, Proline, Threonine, Methylisothiazolinone, Histidine, Phenylalanine, Perilla Ocymoides Leaf Extract, Green 3, Blue 1.
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INGREDIENTS AND APPEARANCE
SATINIQUE ANTI DANDRUFF
pyrithione zinc creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10056-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 9.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) GLYCOL DISTEARATE (UNII: 13W7MDN21W) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) GLYCERETH-26 (UNII: NNE56F2N14) CERAMIDE 2 (UNII: C04977SRJ5) CERAMIDE 3 (UNII: 4370DF050B) CREATINE (UNII: MU72812GK0) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM CHLORIDE (UNII: 451W47IQ8X) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) HYPROMELLOSES (UNII: 3NXW29V3WO) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) ZINC CHLORIDE (UNII: 86Q357L16B) HECTORITE (UNII: 08X4KI73EZ) EDETATE SODIUM (UNII: MP1J8420LU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) PPG-12-BUTETH-16 (UNII: 58CG7042J1) TROLAMINE (UNII: 9O3K93S3TK) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) SODIUM LACTATE (UNII: TU7HW0W0QT) ARGININE (UNII: 94ZLA3W45F) ASPARTIC ACID (UNII: 30KYC7MIAI) PIDOLIC ACID (UNII: SZB83O1W42) GLYCINE (UNII: TE7660XO1C) ALANINE (UNII: OF5P57N2ZX) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) SERINE (UNII: 452VLY9402) VALINE (UNII: HG18B9YRS7) BEHENIC ACID (UNII: H390488X0A) CHOLESTEROL (UNII: 97C5T2UQ7J) ISOLEUCINE (UNII: 04Y7590D77) PROLINE (UNII: 9DLQ4CIU6V) THREONINE (UNII: 2ZD004190S) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) HISTIDINE (UNII: 4QD397987E) PHENYLALANINE (UNII: 47E5O17Y3R) PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10056-006-01 280 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/29/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 03/29/2017 Labeler - Access Business Group LLC (839830713)