2 in 1 Dandruff

2 in 1 Dandruff is an FDA-registered drug product whose active ingredient is PYRITHIONE ZINC. It is labelled by Aldi, Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 64024-311, application M032, label effective 20260513. 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: helps prevent, recurrence flaking, itching associated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use helps prevent recurrence of flaking and itching associated with dandruff

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

Warnings For external use only

Adverse Reactions DIST. & SOLD EXCLUSIVELY BY: ALDI, BATAVIA, IL 60510 www.ALDI.us 844-484-0332 ALDI Twice as Nice GUARANTEE item replaced money refunded PLASTIC BOTTLE Widely Recyclable Empty & Discard Pump how2recycle.info

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 2 in 1 Dandruff used for?
Use helps prevent recurrence of flaking and itching associated with dandruff

Who makes 2 in 1 Dandruff?
Aldi, Inc is the labeler of record for 2 in 1 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 2 in 1 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 2 in 1 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 2 in 1 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.