Label: SEBASTIAN PURIST ANTIDANDRUFF- pyrithione zinc shampoo

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

Drug Label Information

Updated October 13, 2023

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  • Active ingredients

    Pyrithione Zinc 1%

  • Purpose

    Anti-dandruff

  • Uses

    Helps prevent recurrence of flaking and itching associated with dandruff

  • Warnings

    For external use only.

  • When using this product

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

  • Stop use and ask a doctor if

    condition worsens or does not improve after regular use of this product as directed.

  • Keep out of reach of children.

  • Directions

    For best results use at least twice a week or as directed by a doctor.Apply a small amount evenly over wet scalp and hair. Leave on for several minutes. Rinse well.

  • Inactive ingredients

    inactive ingreds

  • Questions or comments?

    Call 1-800-935-5273

  • PRINCIPAL DISPLAY PANEL

    SEB

    MAN.

    THE PURIST

    ANTI-DANDRUFF SHAMPOO

    PYRITHIONE ZINC

    +Guanana

    PROFESSIONAL

    SEBASTIAN

    250 mL (8.4 FL OZ)

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  • INGREDIENTS AND APPEARANCE
    SEBASTIAN PURIST ANTIDANDRUFF 
    pyrithione zinc shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69282-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CAFFEINE (UNII: 3G6A5W338E)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    PEG-3 DISTEARATE (UNII: 8420ECX438)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LAURETH-8 SULFATE (UNII: YP8U3694P0)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ALLANTOIN (UNII: 344S277G0Z)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MAGNESIUM LAURETH SULFATE (UNII: UKW9G007TZ)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    MAGNESIUM LAURETH-8 SULFATE (UNII: 2OTJ9LF5UA)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69282-008-10250 mL in 1 BOTTLE; Type 0: Not a Combination Product06/27/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03206/27/2019
    Labeler - THE WELLA CORPORATION (001399815)
    Registrant - COTY US LLC (039056361)
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