JASON DANDRUFF RELIEF TREATMENT (SULFUR, SALICYLIC ACID) SHAMPOO [THE HAIN CELESTIAL GROUP, INC]

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JASON DANDRUFF RELIEF TREATMENT (SULFUR, SALICYLIC ACID) SHAMPOO [THE HAIN CELESTIAL GROUP, INC]
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NDC 61995-0302-2
Set ID e0ef085d-5925-4448-b83f-507dd4a70760
Category HUMAN OTC DRUG LABEL
Packager The Hain Celestial Group, Inc
Generic Name
Product Class
Product Number
Application Number PART358H
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  • ACTIVE INGREDIENT

    Sulfur                         2.0%

    Salicylic Acid              2.0%



  • PURPOSE

          

    Sulfur                         2.0%  Controls  Dandruff

    Salicylic Acid              2.0%  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. Store between  40 to 100 degrees F (4 to 38 degrees C).
  • INACTIVE INGREDIENT

    Aqua (Water), Sodium Cocoyl Isothionate, Disodium Cocoamphodiacetate, Stearic Acid,Potassium Cocoyl Glutamate, Glycerin, Sodium Lauroyl Sarcosinate, Cetyl Alcohol, Olea Europaea (Olive) Fruit Oil (1), Pogostemon Cablin (Patchouli) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Simmondsia Chinensis (Jojoba) Seed Oil (1), Camphor, Dimethyl Sulfone (2), Menthol, Methyl Salicylate, Potassium Hydroxide, Sodium PCA, Xanthan Gum, Benzyl Alcohol, Capryloyl Glycine, Undecylenoyl Glycine, Amyl Cinnamal,  Benzyl Benzoate,  Hexyl Cinnamal,  Hydroxycitronellal,  Linalool, Limonene, Fragrance (Parfum)

    (1) Certified Organic Ingredients
    (2) MSM
  • QUESTIONS

    Questions? Visit  www.jason-natural.com or call 1-877-527-Jason-01weekdays from 7am-5pm MST.

  • PRINCIPAL DISPLAY PANEL

    image of front label        image of back label

  • INGREDIENTS AND APPEARANCE
    JASON DANDRUFF RELIEF TREATMENT 
    sulfur, salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61995-0302
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR2.0 g  in 100 g
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2.0 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    PATCHOULI OIL (UNII: F3IN55X5PO)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    JOJOBA OIL (UNII: 724GKU717M)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    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)  
    .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61995-0302-2355 g in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H01/05/2010
    Labeler - The Hain Celestial Group, Inc (858894996)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Hain Celestial Group, Inc858894996manufacture
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