FDA Label for Control Dandruff Therapy
View Indications, Usage & Precautions
Control Dandruff Therapy Product Label
The following document was submitted to the FDA by the labeler of this product Kamedis. 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.
Drug Facts
Active Ingredient
Pyrithione Zinc 1.0%
Purpose
Anti-Dandruff
Use
- Helps eliminate scalp itching, irritation, redness, flaking, and scaling associated with dandruff
Warnings
For external use only
When Using This Product
- Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
- If condition worsens or does not improve after regular use of this product as directed, consult a doctor
Keep Out Of Reach Of Children
- If swallowed, get medical help or contact a Poison Control Center right away
Directions
- Apply to wet hair
- Gently massage into hair and scalp and leave for 2-3 minutes before thoroughly rinsing
- Rinse and repeat if desired
- For best results use at least twice a week or as directed by your doctor
Inactive Ingredients
Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Fragrance, Polyquaternium-10, Salicylic Acid, Salt(Sodium Chloride), Soapberry (Sapindus Mukurossi) Fruit Extract, Sodium Benzoate, Sodium Lauroyl Sarcosinate, Triethanolamine, Water.
Questions Or Comments?
1-855-626-6606
Carton Label
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