Mizani Scalp Care Antidandruff

PYRITHIONE ZINC TOPICAL HUMAN OTC DRUG

Mizani Scalp Care Antidandruff is an FDA drug label for the active ingredient PYRITHIONE ZINC manufactured by L'Oreal USA Products Inc administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231211.

Generic name
PYRITHIONE ZINC
Manufacturer
L'Oreal USA Products Inc
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
49967-388
Application
M032
Label effective
20231211

About this product

Mizani Scalp Care Antidandruff is an FDA-registered drug product whose active ingredient is PYRITHIONE ZINC. It is labelled by L'Oreal USA Products Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 49967-388, application M032, label effective 20231211. 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.

What it is used for

Across FDA labelling, products containing PYRITHIONE ZINC are most often described in connection with: helps eliminate, recurrence scalp, flaking scaling, itching associated. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Pyrithione zinc 1%

Indications & Usage

Use helps eliminate recurrence of scalp flaking, scaling, and itching associated with dandruff

Dosage & Administration

Directions • for best results use at least twice a week or as directed by a physician • shake well • wet hair and apply 1 - 2 ounces throughout entire head • massage vigorously • leave on scalp 1 to 3 minutes • rinse well • repeat if necessary

Warnings

Warnings For external use only

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How products containing PYRITHIONE ZINC compare

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.

Dosage formProductsManufacturerProducts
— — The Procter & Gamble Manufacturing Company 10
— — Wal-Mart Stores, Inc. 7
— — L'Oreal USA Products Inc 6
— — J. Strickland & Co. 5
— — Apollo Health and Beauty Care 4

Frequently asked questions

What is Mizani Scalp Care Antidandruff used for?
Use helps eliminate recurrence of scalp flaking, scaling, and itching associated with dandruff

Who makes Mizani Scalp Care Antidandruff?
L'Oreal USA Products Inc is the labeler of record for Mizani Scalp Care Antidandruff. 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 Mizani Scalp Care Antidandruff 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 Mizani Scalp Care Antidandruff 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 Mizani Scalp Care Antidandruff 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.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.