Label: EVERYDAY CLEAN- pyrithione zinc shampoo

  • NDC Code(s): 63148-417-40
  • Packager: Apollo Health and Beauty Care
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 27, 2023

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  • Active Ingredient

    Pyrithione Zinc 1%

  • Purpose

    Anti-dandruff

  • Use

    To help 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 throughly 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

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • Directions

    • For Best results, use at least twice a week or as directed by a doctor.
    • Wet hair, massage onto scalp and rinse.
    • repeat if desired.
  • Inactive Ingredients

    Water (Aqua), Sodium Laureth Sulfate, Acrylates Copolymer, Cocamidopropyl Betaine, Sodium Chloride, Glycol Distearate, Fragrance (Parfum), Laureth-4, Polyquaternium-113, Sodium Hydroxide, Zinc Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CL 42090), Red 33 (Cl 17200.

  • Principal Display Panel

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    EVERYDAY CLEAN 
    pyrithione zinc shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-417
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ZINC CHLORIDE (UNII: 86Q357L16B)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    DIRECT BLUE 1 (UNII: 8NN34MAQ6H)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    LAURETH-4 (UNII: 6HQ855798J)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63148-417-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03211/01/2023
    Labeler - Apollo Health and Beauty Care (201901209)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(63148-417)
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