FDA Label for Divine Dandrene 1%
View Indications, Usage & Precautions
Divine Dandrene 1% Product Label
The following document was submitted to the FDA by the labeler of this product Ds Healthcare Group, 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
Zinc Pyrithione 1%
Purpose
Anti-dandruff
Uses
Relieves and helps prevent recurrence of scalp itch, irritation, redness, flaking and scaling associated with dandruff
Warnings
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 as directed
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away
Otc - Keep Out Of Reach Of Children
Directions
Apply shampoo to wet hair and scalp with gentle massage, leave in for 2-3 minutes, rinse
For best results use atleast 2 times per week or as direacted by a doctor
For maximum benefits use 4-5 times a week along with Dandrene anti-dandruff conditioner
Inactive Ingredients
Water, Disodium Laureth Sulfosuccinate, Triethanolamine, Glycolic Acid, Cocamide MEA, Sodium Lauroyl Sarcosinate, Sodium Lauryl Suloacetate, Glycol Distearate, PEG-150 Distearate, Magnesium Aluminum Silicate, Sodium Citrate, Hexamidine Diisethionate, Hydrolyzed Lupine
Protein, Caprylyl Glycol, Phenoxyethanol, Butylene Glycol, Punica Granatum Extract, Rosmarinus Officinalis Leaf Extract, Shikimic Acid, Tioxolone, Blue 1
Product Label
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