FDA Label for Dzul Anti-dandruff
View Indications, Usage & Precautions
Dzul Anti-dandruff Product Label
The following document was submitted to the FDA by the labeler of this product Caball Sales, 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
Zinc Pyrithione 1%
Otc - Purpose
Anti-Dandruff
Indications & Usage
For the relief of the symptoms of dandruff.
Warnings
For external use only.
Do not use on wounds or damaged skin or on a child under 12 years of age unless directed by a physician.
Otc - When Using
Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
Otc - Stop Use
Conditions worsens or does not improve after regular use of this product as directed.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact Poison Control Center right away.
Dosage & Administration
Apply a small amount quantity of the product into hair and massage the scalp.
Rinse thoroughly with enough water, repeat if needed.
For best results, use at least twice a week or as directed by a doctor.
Other Safety Information
See on the bottom of the bottle for lot number and expiration date.
Inactive Ingredient
Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Acrylates Copolymer, Cocamide MEA, Cocamidopropylamine Oxide, Caprylyl Glycol, Hexylene Glycol, Fragrance (Parfum), Polyquaternium-7, Sodium Hydroxide, Disodium EDTA, Citric Acid, Panthenol, Phenoxyethanol, FD&C Blue No.1 (CI 42090), Hexyl Cinnamal, Benzyl Salicylate, Coumarin, Alpha-Isomethyl Ionone, Geraniol, Linalool.
Otc - Questions
QUESTION OR COMMENTS?
Call (305)-900-8256
* Please review the disclaimer below.