DERMFREE WART CORN REMOVER
DERMFREE WART CORN REMOVER is an FDA drug label for the active ingredient SALICYLIC ACID 40% WART CORN REMOVER manufactured by Jiangxi Yudexi 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 20260723.
- Generic name
- SALICYLIC ACID 40% WART CORN REMOVER
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85248-123
- Application
- M017
- Label effective
- 20260723
About this product
DERMFREE WART CORN REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 40% WART CORN REMOVER. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-123, application M017, label effective 20260723. It is one of 4 FDA drug label records sharing the active ingredient SALICYLIC ACID 40% WART CORN 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 40% WART CORN REMOVER are most often described in connection with: removal warts. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use For the removal of warts and corns.
Dosage & Administration
Directions Wash the affected area. (Optional: soak the wart in warm water for 5 minutes.)Dry the area thoroughly. If needed, cut the plaster to fit the wart. Apply the medicated plaster. Repeat every 48 hours as needed, for up to 12 weeks.Other information: Store between 59°F and 86°F(15°C and 30°C).
Warnings
Warnings For external use only.
More products with the same ingredient
SALICYLIC ACID 40% WART CORN REMOVERHEALMUSZ WART CORN REMOVER
View labelLixuhya Liquid SKIN WART CORN REMOVER
View labelSANUSCODE WART CORN REMOVER
View labelHow products containing SALICYLIC ACID 40% WART CORN REMOVER compare
FDA lists 4 drug label records with SALICYLIC ACID 40% WART CORN 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 | 3 |
| — | — | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is DERMFREE WART CORN REMOVER used for?
Use For the removal of warts and corns.
Who makes DERMFREE WART CORN REMOVER?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for DERMFREE WART CORN REMOVER. 4 FDA label records share the active ingredient SALICYLIC ACID 40% WART CORN 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 DERMFREE WART CORN 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 DERMFREE WART CORN 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 40% WART CORN REMOVER?
Yes. 4 FDA drug label records list SALICYLIC ACID 40% WART CORN 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 DERMFREE WART CORN 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.