Label: NATURALTECH PURIFYING ANTI-DANDRUFF- pyrithione zinc gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • Active Ingredient

    Zinc Pyrithione 0,48%

  • Purpose

    Antidandruff

  • Uses

    For relief of the symptoms of dandruff

  • Warnings

    For external use only

  • Stop use and ask a doctor if

    condition worsens or does not improve after regular use

  • When using this product

    keep out of eyes. Rinse with water to remove.

  • Keep out of reach of children

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

  • Directions

    • Spread carefully over the whole scalp, or only on areas affected by dandruff, massaging in gently.
    • Leave to process for 10 minutes.
    • Rinse thoroughly.
    • For best results use at least twice a week or as directed by a doctor.
  • Other information

    • you may report a serious adverse event from using this product to Report Reaction, LLC PO Box 22, Plainsboro, NJ
  • Inactive Ingredients

    Water, Polysorbate 20, Pentasodium Pentetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Propylene Glycol, Glycerin, Bisabolol, Piroctone Olamine, Taraxacum Officinale (Dandelion) Root Extract, Tocopherol, Tetrasodium EDTA, Sodium Hydroxide, Linalool, Fragrance.

  • PRINCIPAL DISPLAY PANEL - 150 mL Bottle Carton Label

    NATURALTECH™

    PURIFYING ANTI-DANDRUFF GEL

    TREATMENT FOR SCALP WITH

    OILY OR DRY DANDRUFF

    WITH DANDELION PHYTOCEUTICALS

    150 mL 5.07 Fl. Oz.

    davines

    gel

  • INGREDIENTS AND APPEARANCE
    NATURALTECH PURIFYING ANTI-DANDRUFF 
    pyrithione zinc gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64724-1017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC0.48 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    PIROCTONE OLAMINE (UNII: A4V5C6R9FB)  
    TARAXACUM OFFICINALE (UNII: 39981FM375)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64724-1017-11 in 1 CARTON02/29/2012
    1150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03202/29/2012
    Labeler - Davines S.p.A. (430193664)
    Registrant - Davines S.p.A. (430193664)
    Establishment
    NameAddressID/FEIBusiness Operations
    Biokosmes SRL436948830manufacture(64724-1017)
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