Active Ingredient
Pyrithione Zinc 1%
Topcare Everyday Clean Dandruff
FDA Label NDC 36800-795
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates Llc for the product Topcare Everyday Clean Dandruff (NDC 36800-795). 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 active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antidandruff
Use
to help prevent recurrence of flaking and itching associated with dandruff.
Warnings
For external use only
When Using This Product
avoid contact with eyes. If contact occurs, rinse 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.
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
- for best results, use at least twice a week or as directed by a doctor
- wet hair, massage onto scalp and rinse
- repeat if desired
Inactive Ingredients
Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Acrylates Copolymer, Glycol Distearate, Cocamidopropyl Betaine, Laureth-4, Fragrance (Parfum), Sodium Hydroxide, Tetrasodium EDTA, Cocamide MEA, Methylchloroisothiazolinone, Methylisothiazolinone, Red 33 (CI 17200), Blue 1 (CI 42090).
Labe Copy
Image Of The Label (23654)
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