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Jason Dandruff Relief Treatment 2 in 1 (The Hain Celestial Group, Inc)

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SHAMPOO 355 g in 1 BOTTLE (61995-0029-2) Label Information

Complete Jason Dandruff Relief Treatment 2 in 1 Information

  • ACTIVE INGREDIENT

    Zinc Pyrithiopne                 1.0%





  • PURPOSE

          

      Controls  Dandruff


                   



  • 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

    • Gently massage a quarter-sized dollop onto wet scalp.
    • Leave on for 2-3 minutes.
    • Rinse throughly with tepid water.
    • For good results use every other day.
    • For maintenance use one or two treatment per week
     
    Store between  40 to 100 degrees F (4 to 38 degrees C).
  • INACTIVE INGREDIENT

    Aqua (Water), Lauryl Glucoside, Glycerin, Sodium Coco-Sulfate, Sodium Cocoyl Isothionate, Glycol Stearate,Cetyl Alcohol, Olea Europaea (Olive) Fruit Oil (1), Simmondsia Chinensis (Jojoba) Seed Oil (1), Babassu Oil Polyglyceryl-4 Esters, Coco-Glucoside, Hydrolyzed Wheat Protein, Glyceryl Oleate, Magnesium Sulfate, Polyquaternium-10, Sodium PCA,Sodium Sulfate, Zinc Carbonate, Benzyl Alcohol,Alpha-Isomethyl Ionone, Butylphenyl Methylpropional, Fragrance (Parfum).

    (1) Certified Organic Ingredients


  • 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 2 IN 1  
    zinc pyrithione shampoo
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:61995-0029
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1.0 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM COCO-SULFATE (UNII: 3599J29ANH)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    BABASSU OIL (UNII: 8QSB4M5477)  
    HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    JOJOBA OIL (UNII: 724GKU717M)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    ZINC CARBONATE (UNII: EQR32Y7H0M)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:61995-0029-2 355 g in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part358H 04/19/2012
    Labeler - The Hain Celestial Group, Inc (858894996)
    Establishment
    Name Address ID/FEI Business Operations
    The Hain Celestial Group, Inc 858894996 manufacture