FDA Label for Dry Scalp Care Dandruff Md
View Indications, Usage & Precautions
Dry Scalp Care Dandruff Md Product Label
The following document was submitted to the FDA by the labeler of this product Blue Coss Laboratories, 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
Active Ingredient Purpose
Pyrithione Zinc 1% anti-dandruff
Otc - Purpose
Use: Helps prevent recurrence of flaking and itching associated with dandruff
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.
Indications & Usage
Stop use and ask a doctor if
condition worsens or does not improve after regular use as directed.
Warnings
Warnings: For external use only.
When using this product: Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
Dosage & Administration
Directions:
Shake well.
For maximum dandruff control, use every time you shampoo.
Wet Hair, massage onto scalp, rinse, repeat if desired.
For best results use at least twice a week or as directed by a doctor.
Inactive Ingredient
Inactive Ingredients: Aqua, Sodium Laureth Sulphate, Cocomide DEA, Sodium Chloride Zinc Pyrithione, Cocamidopropyl Betaine, Glycol Distearate, Glycerin, Polyquaternum-7, Propylene Glycol, Parfum, Guar Gum, DMDM Hydantoin, Disodium EDTA, Citric Acid CI 42090
Package Label.Principal Display Panel
Dandruff MD Shampoo 12 FL. OZ. (354 ML)
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