Label: SATINIQUE ANTI DANDRUFF- pyrithione zinc cream

  • NDC Code(s): 10056-006-01
  • Packager: Access Business Group LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 23, 2023

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  • Drug Facts

  • Active Ingredients

    Pyrithione Zinc 0.95%

    Purpose

    Anti Dandruff

  • Uses

    • Controls symptoms of dandruff
  • Warnings

    For external use only.

    If contact occurs, rinse eyes thoroughly with water. Avoid contact with eyes.

    or does not improve after regular use, consult a doctor. If condition worsens

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Shake well before use.
    • Wet hair. Apply shampoo and work into a lather. Rinse thoroughly.
    • For best result, use at least twice a week or as directed by a doctor.
  • 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.

  • Package Labeling:

    Label3

  • INGREDIENTS AND APPEARANCE
    SATINIQUE ANTI DANDRUFF 
    pyrithione zinc cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10056-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC9.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10056-006-01280 mL in 1 BOTTLE; Type 0: Not a Combination Product03/29/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03203/29/2017
    Labeler - Access Business Group LLC (839830713)
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