Label: LOREAL PARIS EVER PURE DANDRUFF SCALP CARE AND DETOX- pyrithione zinc shampoo

  • NDC Code(s): 49967-056-01
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • Active ingredient

    Pyrithone zinc 1%

  • Purpose

    Antidandruff

  • Use

    helpls prevent recurrence of scalp flaking and itching associated with 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

  • 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 wet hair by gently massaging onto scalp and hair
    • rinse well
  • Inactive ingredients

    water, cocamidopropyl betaine, disodium laureth sulfosuccinate, sodium lauryl sulfoacetate, decyl glucoside, sodium lauroyl sarcosinate, glycol distearate, sodium chloride, coco-betaine, fragrance, amodimethicone, PPG-5-ceteth-20, acrylates copolymer, sodium benzoate, carbomer, PEG-55 propylene glycol oleate, propylene glycol, polyquaternium-39, menthol, hydrogenated starch hydrolysate, benzoic acid, trideceth-6, butylene glycol, citronellol, sodium polynaphthalenesulfonate, linalool, limonene, geraniol, cetrimonium chloride, citral, cellulose gum, tetrasodum EDTA, aphanizomenon flos-aquae extract, melia azadirachta leaf extract, methylisothiazolinone, phenoxyethanol, potassium sorbate

  • Questions or comments?

    1-800-631-7358

  • PRINCIPAL DISPLAY PANEL

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  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    LOREAL PARIS EVER PURE DANDRUFF SCALP CARE AND DETOX 
    pyrithione zinc shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-056
    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)  
    PPG-5-CETETH-20 (UNII: 4AAN25P8P4)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYQUATERNIUM-39 (22.5/51/26.5 ACRYLIC ACID/ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: X2NH1K9F8K)  
    MENTHOL (UNII: L7T10EIP3A)  
    HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    GERANIOL (UNII: L837108USY)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    CITRAL (UNII: T7EU0O9VPP)  
    CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 150 MPA.S AT 1%) (UNII: 99H65D77XY)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    APHANIZOMENON FLOSAQUAE (UNII: 49VG1X560X)  
    AZADIRACHTA INDICA LEAF (UNII: HKY915780T)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-056-01250 mL in 1 TUBE; Type 0: Not a Combination Product07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03207/01/2020
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.960317444manufacture(49967-056) , pack(49967-056)
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