Label: J1003005 JASON DANDRUFF RELIEF- sulfur, salicylic acid shampoo

  • NDC Code(s): 61995-0030-8
  • Packager: The Hain Celestial Group, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 31, 2024

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  • ACTIVE INGREDIENT

    Sulfur 2.4%

    Salicylic Acid 2.2%



  • PURPOSE


    Sulfur Controls Dandruff

    Salicylic Acid Controls Seborrheic Dermatitis



  • INDICATIONS & USAGE

    • Controls recurrence of flaking, scaling and itching associated with dandruff
    • Helps prevent seborrheic dermatitis
  • WARNINGS

    For external use only . Avoid contact with eyes.Rinse eyes throughly with water in case contact occurs.Discontinue use and consult your physician if irritation develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed get medical help or contact Poison Center right away.

  • DOSAGE & ADMINISTRATION

    For best results, use at least three times each week. Wet hair and lather,massage into scalp. Rinse and repeat if desired.

  • INACTIVE INGREDIENT

    Water (Aqua), Potassium Cocoyl Glutamate, Sodium Cocoyl Isethionate, Cetyl Alcohol, Disodium Cocoamphodiacetate, Cocamidopropyl Betaine, Stearic Acid, Glycerin, Glyceryl Stearate SE, Sodium Laurylglucosides Hydroxypropylsulfonate, Olea Europaea (Olive) Fruit Oil (1), Rosmarinus Officinalis (Rosemary) Leaf Oil, Simmondsia Chinensis (Jojoba) Seed Oil (1), Chenopodium Quinoa Seed (1), Camphor, Capryloyl Glycine, Disodium Cocoyl Glutamate, Maltodextrin, Menthol, Methyl Salicylate, Potassium Hydroxide, Sodium Chloride, Sodium PCA, Triethyl Citrate, Undecylenoyl Glycine, Xanthan Gum, Alcohol (1), Benzyl Alcohol, Linalool

    (1) Certified Organic Ingredients

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    J1003005 JASON DANDRUFF RELIEF 
    sulfur, salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61995-0030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR2.4 g  in 100 g
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURYLGLUCOSIDES HYDROXYPROPYLSULFONATE (UNII: Z6GFR7R72Y)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    JOJOBA OIL (UNII: 724GKU717M)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    MENTHOL (UNII: L7T10EIP3A)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    UNDECYLENOYL GLYCINE (UNII: 4D20464K2J)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    ALCOHOL (UNII: 3K9958V90M)  
    POTASSIUM COCOYL GLUTAMATE (UNII: IR5T90R7LZ)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61995-0030-8355 g in 1 BOTTLE; Type 0: Not a Combination Product11/27/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03211/27/2017
    Labeler - The Hain Celestial Group, Inc. (117115556)
    Registrant - The Hain Celestial Group, Inc. (081512382)