Label: HEAD AND SHOULDERS SUPREME CLARIFY AND VOLUMIZE- pyrithione zinc shampoo

  • NDC Code(s): 69423-638-35
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    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 this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • for best results use at least twice a week or as directed by a doctor.
    • for maximum dandruff control, use every time you shampoo.
    • shake before use.
    • wet hair, massage onto scalp, rinse, repeat if desired.
  • Inactive Ingredients

    Water, lauramidopropyl betaine, sodium cocoyl isethionate, sodium lauroyl sarcosinate, sodium chloride, argania spinosa kernel oil, spirulina platensis extract, sodium citrate, acrylates copolymer, polyquaternium-10, fragrance, citric acid, sodium benzoate,
    sodium salicylate.

  • Questions (or comments)?

    1-800-723-9569

  • SPL UNCLASSIFIED SECTION

    Dist. by PROCTER & GAMBLE,
    CINCINNATI, OH 45202

  • Principal display panel - 350 mL Bottle Label

    head &
    shoulders ®

    PYRITHIONE ZINC DANDRUFF

    SCALP & HAIR SHAMPOO

    SUPREME

    CLARIFY &

    VOLUMIZE

    WITH ARGAN OIL & BLUE GREEN ALGAE EXTRACT

    FREE FROM SULFATES

    PARABENS

    DYES

    PHOSPHATES

    SILICONES

    11.8 FL OZ
    (350 mL

    HS

  • INGREDIENTS AND APPEARANCE
    HEAD AND SHOULDERS SUPREME CLARIFY AND VOLUMIZE 
    pyrithione zinc shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-638
    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
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM SALICYLATE (UNII: WIQ1H85SYP)  
    LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS)  
    SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-638-35350 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/22/202205/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03201/22/202205/01/2025
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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