Label: KERASTASE PARIS SYMBIOSE ANTIDANDRUFF- pyrithione zinc shampoo

  • NDC Code(s): 49967-871-01, 49967-871-02, 49967-871-03
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 24, 2024

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  • Active ingredient

    Pyrithione zinc 1%

  • Purpose

    Antidandruff

  • Uses

    • helps eliminate the symptoms of dandruff
  • Warnings

    For external use only

  • When using this product

    avoid contact with the 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.

    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 
    • apply to hair
    • massage
    • rinse
  • Inactive ingredients

    water, cocamidopropyl betaine, disodium laureth sulfosuccinate, sodium lauryl sulfoacetate, decyl glucoside, sodium lauroyl sarcosinate, glycol distearate, sodium chloride, coco-betaine, fragrance, amodimethicone, citric acid, PPG-5-ceteth-20, sodium hydroxide, acrylates copolymer, sodium benzoate, carbomer, PEG-55 propylene glycol oleate, propylene glycol, polyquaternium-39, limonene, squalane, menthol, glycerin, benzoic acid, trideceth-6, sodium polynaphthalenesulfonate, benzyl salicylate, salicylic acid, benzyl alcohol, linalool, citronellol, citral, geraniol, cetrimonium chloride, cellulose gum, artemisia umbelliformis flower extract, tetrasodium EDTA, methylisothiazolinone, potassium sorbate

  • PRINCIPAL DISPLAY PANEL

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  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    KERASTASE PARIS SYMBIOSE ANTIDANDRUFF 
    pyrithione zinc shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-871
    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
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    AMODIMETHICONE (1300 CST) (UNII: 3V7U636DWN)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PPG-5-CETETH-20 (UNII: 4AAN25P8P4)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    PEG-55 PROPYLENE GLYCOL OLEATE (UNII: 7RDE7PJS40)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYQUATERNIUM-39 (35/35/30 ACRYLIC ACID/ACRYLAMIDE/DADMAC; 1500000 MW) (UNII: EOD3UE785A)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    SQUALANE (UNII: GW89575KF9)  
    MENTHOL (UNII: L7T10EIP3A)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    CITRAL (UNII: T7EU0O9VPP)  
    GERANIOL (UNII: L837108USY)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    ARTEMISIA UMBELLIFORMIS FLOWER (UNII: 91OLL9AJ7D)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-871-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product12/12/202201/31/2025
    2NDC:49967-871-02250 mL in 1 BOTTLE; Type 0: Not a Combination Product12/12/202204/30/2025
    3NDC:49967-871-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product12/12/202201/31/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03212/12/202204/30/2025
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'OREAL USA, INC960317444manufacture(49967-871) , pack(49967-871)
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