RENUEVO ANTI-DAMDRUFF
RENUEVO ANTI-DAMDRUFF is an FDA drug label for the active ingredient ZINC PYRITHIONE manufactured by LEON UP GLOBAL HOLDING CORP 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 20260605.
- Generic name
- ZINC PYRITHIONE
- Manufacturer
- LEON UP GLOBAL HOLDING CORP
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87708-002
- Application
- M032
- Label effective
- 20260605
About this product
RENUEVO ANTI-DAMDRUFF is an FDA-registered drug product whose active ingredient is ZINC PYRITHIONE. It is labelled by LEON UP GLOBAL HOLDING CORP taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87708-002, application M032, label effective 20260605. It is one of 3 FDA drug label records sharing the active ingredient ZINC PYRITHIONE. 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 ZINC PYRITHIONE 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.
Active ingredients
Indications & Usage
Helps prevent recurrence of flaking and itching associated with dandruff
Dosage & Administration
Wet hair. Shake well. Massage shampoo into scalp. Rinse. Repeat if desired. For best results, use at least twice a week or as directed by a doctor. For maximum dandruff control, use every time you shampoo.
Warnings
For external use only Do not use on wounds or damaged skin or on a child under 12 years of age unless directed by a physician.
More products with the same ingredient
ZINC PYRITHIONEHow products containing ZINC PYRITHIONE compare
FDA lists 3 drug label records with ZINC PYRITHIONE 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 form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | LEON UP GLOBAL HOLDING CORP | 1 |
| — | — | MEERAY COSMETICS CO., LTD. | 1 |
| — | — | Zero Flakes Given, Inc. | 1 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is RENUEVO ANTI-DAMDRUFF used for?
Helps prevent recurrence of flaking and itching associated with dandruff
Who makes RENUEVO ANTI-DAMDRUFF?
LEON UP GLOBAL HOLDING CORP is the labeler of record for RENUEVO ANTI-DAMDRUFF. 3 FDA label records share the active ingredient ZINC PYRITHIONE, 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 RENUEVO ANTI-DAMDRUFF 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 RENUEVO ANTI-DAMDRUFF 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 ZINC PYRITHIONE?
Yes. 3 FDA drug label records list ZINC PYRITHIONE 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 RENUEVO ANTI-DAMDRUFF 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.