OTC Medication Information: J1002901Jason Dandruff Relief 2in1Treatment

J1002901JASON DANDRUFF RELIEF 2IN1TREATMENT- pyrithione zinc shampoo
The Hain Celestial Group, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Zinc Pyrithiopne 1.0%

Controls Dandruff

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

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. If swallowed get medical help or contact Poison Center right away.

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

Water (Aqua), Sodium Cocoyl Isethionate, Cetyl Alcohol, Glycerin, Cocamidopropyl Hydroxysultaine, Sodium Laurylglucosides Hydroxypropylsulfonate, Sodium Cocoyl Glutamate, Sodium Chloride, Glyceryl Stearate SE, Coco-Glucoside, Glyceryl Oleate, Butyrospermum Parkii (Shea) Butter Unsaponifiables, Citrus Aurantium Dulcis (Orange) Peel Oil, Olea Europaea (Olive) Fruit Oil (1), Simmondsia Chinensis (Jojoba) Seed Oil (1), Soybean Glycerides, Chenopodium Quinoa Seed (1), Ascorbyl Palmitate, Babassu Oil Polyglyceryl-4 Esters, Benzyl Acetate, Caprylic/Capric Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Cellulose Gum, Citric Acid, Diheptyl Succinate, Guar Hydroxypropyltrimonium Chloride, Phenethyl Alcohol, Sodium Hydroxide, Sodium PCA, Terpineol, Triethyl Citrate, Xanthan Gum, Zinc Carbonate, Alcohol (1), Ethylhexylglycerin, Phenoxyethanol, Potassium Sorbate, Limonene, Linalool.

(1) Certified Organic Ingredients

J10029 Label
(click image for full-size original)

J1002901JASON DANDRUFF RELIEF 2IN1TREATMENT
zinc pyrithione shampoo
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:61995-0129
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC 1 g in 100 g
Inactive Ingredients
Ingredient Name Strength
GLYCERYL OLEATE
SODIUM COCOYL GLUTAMATE
SODIUM DECYLGLUCOSIDES HYDROXYPROPYLSULFONATE
SODIUM HYDROXIDE
TRIETHYL CITRATE
ETHYLHEXYLGLYCERIN
PHENOXYETHANOL
POTASSIUM SORBATE
CAPRYLIC/CAPRIC ACID
OLIVE OIL
CELLULOSE, MICROCRYSTALLINE
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)
TERPINEOL
XANTHAN GUM
STEARYL ALCOHOL
WATER
SODIUM COCOYL ISETHIONATE
GLYCERIN
CETYL ALCOHOL
BABASSU OIL
JOJOBA OIL
ZINC CARBONATE
DIHEPTYL SUCCINATE
ASCORBYL PALMITATE
COCAMIDOPROPYL HYDROXYSULTAINE
SODIUM CHLORIDE
ANHYDROUS CITRIC ACID
MEDIUM-CHAIN TRIGLYCERIDES
ORANGE OIL
GLYCERYL STEARATE SE
CHENOPODIUM QUINOA SEED
ALCOHOL
BENZYL ACETATE
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)
ORANGE PEEL
COCO GLUCOSIDE
SHEA BUTTER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:61995-0129-8 355 g in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 11/27/2017
Labeler — The Hain Celestial Group, Inc. (117115556)
Registrant — The Hain Celestial Group, Inc. (081512382)
Establishment
Name Address ID/FEI Operations
The Hain Celestial Group, Inc 081512382 manufacture (61995-0129)

Revised: 04/2021 The Hain Celestial Group, Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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