Musizlee WART REMOVER
Musizlee WART REMOVER is an FDA drug label for the active ingredient SALICYLIC ACID 1% WART REMOVER manufactured by Wenzhou Yuyuan Pharmaceutical Co., Ltd. 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 20260616.
- Generic name
- SALICYLIC ACID 1% WART REMOVER
- Manufacturer
- Wenzhou Yuyuan Pharmaceutical Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87786-004
- Application
- M028
- Label effective
- 20260616
About this product
Musizlee WART REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 1% WART REMOVER. It is labelled by Wenzhou Yuyuan Pharmaceutical Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87786-004, application M028, label effective 20260616. It is one of 22 FDA drug label records sharing the active ingredient SALICYLIC ACID 1% WART REMOVER. 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 SALICYLIC ACID 1% WART REMOVER are most often described in connection with: helps improve, appearance common, warts flat, smooth skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Helps improve the appearance of common warts, flat warts and moles, and smooth skin texture.
Dosage & Administration
Directions 1.Use after cleansing and toning your skin. 2.Apply the serum to the affected area twice daily, for a minimum of 4 weeks. 3.Continue use until warts and moles are no longer visible.
Warnings
Warnings For external use only.
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View labelHow products containing SALICYLIC ACID 1% WART REMOVER compare
FDA lists 22 drug label records with SALICYLIC ACID 1% WART REMOVER 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 |
|---|---|---|---|
| — | — | Jiangxi Yudexi Pharmaceutical Co., LTD | 15 |
| — | — | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 6 |
| — | — | Jiangxi Zhongletang Pharmaceuticals Co.,Ltd. | 1 |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Musizlee WART REMOVER used for?
Uses Helps improve the appearance of common warts, flat warts and moles, and smooth skin texture.
Who makes Musizlee WART REMOVER?
Wenzhou Yuyuan Pharmaceutical Co., Ltd. is the labeler of record for Musizlee WART REMOVER. 22 FDA label records share the active ingredient SALICYLIC ACID 1% WART REMOVER, 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 Musizlee WART REMOVER 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 Musizlee WART REMOVER 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 SALICYLIC ACID 1% WART REMOVER?
Yes. 22 FDA drug label records list SALICYLIC ACID 1% WART REMOVER 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 Musizlee WART REMOVER 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.