JASON DANDRUFF RELIEF TREATMENT 2 IN 1- zinc pyrithione shampoo

Jason Dandruff Relief Treatment 2 in 1 by

Drug Labeling and Warnings

Jason Dandruff Relief Treatment 2 in 1 by is a Otc medication manufactured, distributed, or labeled by The Hain Celestial Group, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

     

          

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