Label: MD CELL SCALP- pyrithione zinc, panthenol, niacinamide, menthol, salicylic acid shampoo

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated August 26, 2016

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  • Active ingredients

    Pyrithione zinc (0.9%)

    Panthenol (0.5%)

    Niacinamide (0.3%)

    Salicylic Acid (0.01%)

  • PURPOSE

    anti-dandruff

    hair tonic

    antiseborrheic

  • Keep out of reach of children

     Do not swallow. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

  • Uses

    Helps prevent hair loss and thicken hair. Keeps scalp clean, healthy and smooth.

  • Warnings

    For external use only
    Do not use on damaged or broken scalp
    When using this product
    - Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
    Stop use and ask doctor if rash or irritation on scalp develops and lasts.

    Store at room temperature

  • Directions

    After wet hair with lukewarm water, apply the adequate amount on scalp and hair and massage gently until having foam enough. After 3 min, rinse with clean water.

  • Inactive Ingredients

    Water, Sodium Laureth Sulfate, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Glycerin, Polyquaternium-7, Dimethicone, Cocamide MEA, Sodium Benzoate, Cetrimonium Chloride, Phenoxyethanol, Guar Hydroxypropyltrimonium Chloride, Carbomer, Zinc Chloride, Disodium EDTA, Menthol, Biotin, Trideceth-10, Cocamide DEA , Sophora Angustifolia Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Artemisia Princeps Leaf Extract, Coix Lacryma-Jobi Ma-yuen Seed Extract, Yeast Extract, Bifida Ferment Filtrate, rh-Oligopeptide-1, sh-Polypeptide-9, rh-Polypeptide-3, Copper Tripeptide-1, Citric Acid

  • MD CELL Scalp Shampoo

    md cell scalp shampoo

  • INGREDIENTS AND APPEARANCE
    MD CELL SCALP 
    pyrithione zinc, panthenol, niacinamide, menthol, salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70834-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Pyrithione zinc (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) Pyrithione zinc2.7 g  in 300 mL
    Panthenol (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) Panthenol1.5 g  in 300 mL
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide0.9 g  in 300 mL
    Menthol (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) Menthol0.21 g  in 300 mL
    Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid0.03 g  in 300 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    Ammonium Lauryl Sulfate (UNII: Q7AO2R1M0B)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Glycerin (UNII: PDC6A3C0OX)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    Zinc Chloride (UNII: 86Q357L16B)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Biotin (UNII: 6SO6U10H04)  
    Trideceth-10 (UNII: G624N6MSBA)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)  
    COIX LACRYMA-JOBI VAR. MA-YUEN SEED (UNII: 8DW238I7ZI)  
    YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)  
    NEPIDERMIN (UNII: TZK30RF92W)  
    FIBROBLAST GROWTH FACTOR 7 (UNII: 9YXF283GP1)  
    PREZATIDE COPPER (UNII: 6BJQ43T1I9)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70834-101-021 in 1 PACKAGE07/20/2016
    1NDC:70834-101-01300 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/18/2016
    Labeler - A Joint-stock Corporation GMC Holdings (689847352)
    Registrant - A Joint-stock Corporation GMC Holdings (689847352)
    Establishment
    NameAddressID/FEIBusiness Operations
    A Joint-stock Corporation GMC Holdings689847352manufacture(70834-101)
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