FDA Label for J1003005 Jason Dandruff Relief
View Indications, Usage & Precautions
J1003005 Jason Dandruff Relief Product Label
The following document was submitted to the FDA by the labeler of this product The Hain Celestial Group, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Sulfur 2.4%
Salicylic Acid 2.2%
Otc - 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.
Otc - 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
Aqua (Water), Potassium Cocoyl Glutamate, Sodium Cocoyl Isothionate, Disodium Cocoamphodiacetate, Stearic Acid, Glycerin, Glyceryl Stearate SE, Cetyl Alcohol, Olea Europaea (Olive) Fruit Oil (1), Chenopodium Quinoa Seed (1), Rosmarinus Officinalis (Rosemary) Leaf Oil, Simmondsia Chinensis (Jojoba) Seed Oil (1), Camphor, Menthol, Methyl Salicylate, Potassium Hydroxide, Sodium PCA, Xanthan Gum, Benzyl Alcohol, Capryloyl Glycine, Sodium Chloride, Undecylenoyl Glycine, Linalool.
(1)
Certified Organic Ingredients
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