Dosage & Administration
For maximum dandruff control, use every time you shampoo.
Wet hair, massage unto scalp, rinse, and repeat if desired.
For best results use at least twice a week or as directed by a doctor.
Pyrithione Zinc
FDA Label NDC 50157-125
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brands International for the product Pyrithione Zinc (NDC 50157-125). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, otc - active ingredient, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
For external use only.
Inactive Ingredient
Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Glycol Distearate, Aloe vera Leaf Extract, Parfum, Vitamin E, Methylchloroisothiazolinone,Methylisothiazolinone, FD&C Blue#1 ,FD&C Red#33.
Indications & Usage
Helps prevent recurrence of flaking and itching associated with dandruff.
Otc - Keep Out Of Reach Of Children
Keep Out of children’s reach.
Otc - Purpose
Anti-dandruff
Otc - Active Ingredient
Pyrithione Zinc 0.3%
Otc - Stop Use
Condition worsens or does not improve after regular use of this product as directed
Otc - When Using
Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Package Label.Principal Display Panel
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