FDA Label for Dandruff
View Indications, Usage & Precautions
Dandruff Product Label
The following document was submitted to the FDA by the labeler of this product Xtreme Tools International, 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.
Active Ingredient
Pyrithione zinc 2%
Purpose
Anti-dandruff
Use
Helps prevent itching and flaking associated with dandruff.
Warning
For external use only.
When Using This Product
- Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
- condition worsens or does not improve after regular use of this product.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help, or contact a Poison Control Center right away.
Directions
- shake well
- For best results use at least twice a week or as directed by a doctor
Inactive Ingredients
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Cocamide MEA, Glycol Distearate, Polysorbate 20,PPG-10 Cetyl Ether, PEG-8, Polyquaternium-10, Acrylates, Vinyl Neodecanoate, Crosspolymer, Hydrolyzed Wheat Protein, Ricinus Communis (Castor) Seed Oil, Hydrolyzed Keratin, Chitosan Succinamide, Argania Spinosa (Argan) Kemel Oil, Olea Europaea (Olive) Oil, Sodium Benzoate, Pottassium Sorbate, Fragrance, Citric Acid, CI 42090
Questions Or Comments?
Call 1-305-622-7474, Monday through Friday 9:00 AM to 5:00 PM
Package Label.Principal Display Panel
473 mL in Bottle; NDC 74553-003-01
* Please review the disclaimer below.