Label: ANTI DANDRUFF SHAMPOO473ML- pyrithione zinc liquid

  • NDC Code(s): 85434-005-01
  • Packager: Guangdong Quaker Daily Chemical Co., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 16, 2026

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  • ACTIVE INGREDIENT

    Pyrithione zinc 1%

  • PURPOSE

    Anti-dandruff

  • INDICATIONS & USAGE

    helps prevent recurrence of flaking and itching associated with dandruff.

  • WARNINGS

    For external use only.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. Avoid contact eyes, if contact occurs, rinse thoroughly with water.

  • DOSAGE & ADMINISTRATION

    Shake well before use.
    Massage onto wet scalp, rinse, repeat if desired.
    For best results, use at least twice a week.

  • INACTIVE INGREDIENT

    water
    sodium laureth sulfate
    cocamidopropyl betaine
    guar hydroxypropyltrimonium chloride
    acrylates/c10-30 alkyl acrylate crosspolymer
    zinc chloride
    sodium chloride
    methylchloroisothiazolinone
    dimethicone
    trideceth-3
    trideceth-10
    citric acid
    prunus persica (peach) leaf extract
    trehalose
    aloe barbadensis leaf juice
    ammonium lauryl sulfate
    sodium benzoate
    blue 1 CI 42090

  • PRINCIPAL DISPLAY PANEL

    label2

  • INGREDIENTS AND APPEARANCE
    ANTI DANDRUFF SHAMPOO473ML 
    pyrithione zinc liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85434-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TRIDECETH-3 (UNII: 438A02204X)  
    GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    ZINC CHLORIDE (UNII: 86Q357L16B)  
    TRIDECETH-10 (UNII: G624N6MSBA)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)  
    CI 42090 (UNII: H3R47K3TBD)  
    PRUNUS PERSICA LEAF (UNII: VN3501T41P)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    TREHALOSE (UNII: B8WCK70T7I)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85434-005-01473 mL in 1 BOTTLE; Type 0: Not a Combination Product06/16/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03206/16/2026
    Labeler - Guangdong Quaker Daily Chemical Co., LTD (548075342)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Quaker Daily Chemical Co., LTD548075342manufacture(85434-005)
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