Otc - Active Ingredient
Sulfur 2.0%
Salicylic Acid 2.0%
The following Structured Product Label (SPL) was submitted to the FDA by The Hain Celestial Group, Inc for the product Jason Dandruff Relief Treatment (NDC 61995-0302). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Sulfur 2.0%
Salicylic Acid 2.0%
Sulfur 2.0% Controls Dandruff
Salicylic Acid 2.0% Controls 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.
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)
Questions? Visit www.jason-natural.com or call 1-877-527-Jason-01weekdays from 7am-5pm MST.
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