Dermoia Dandruff

Dermoia Dandruff is an FDA-registered drug product whose active ingredient is PYRITHIONE ZINC. It is labelled by Treasurewise LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83524-965, application M032, label effective 20260422. It is one of 64 FDA drug label records sharing the active ingredient PYRITHIONE ZINC. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing PYRITHIONE ZINC are most often described in connection with: symptoms dandruff. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use(s) For relief of the symptoms of dandruff

Directions: Apply and then wash off after brief (a few minutes) exposure. For best results use at least twice a week or as directed by a doctor.

Warnings: For external use only. When using this product Avoid contact with the 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 a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

FDA lists 64 drug label records with PYRITHIONE ZINC as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Dermoia Dandruff used for?
Use(s) For relief of the symptoms of dandruff

Who makes Dermoia Dandruff?
Treasurewise LLC is the labeler of record for Dermoia Dandruff. 64 FDA label records share the active ingredient PYRITHIONE ZINC, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Dermoia Dandruff come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Dermoia Dandruff prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing PYRITHIONE ZINC?
Yes. 64 FDA drug label records list PYRITHIONE ZINC as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Dermoia Dandruff been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.