Txovis SKIN WART CORN REMOVER
Txovis SKIN WART CORN REMOVER is an FDA drug label for the active ingredient SALICYLIC ACID manufactured by Guangdong Joyan Biological Technology 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 20260819.
- Generic name
- SALICYLIC ACID
- Manufacturer
- Guangdong Joyan Biological Technology Co.,Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85779-005
- Application
- 505G(a)(3)
- Label effective
- 20260819
About this product
Txovis SKIN WART CORN REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID. It is labelled by Guangdong Joyan Biological Technology Co.,Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85779-005, application 505G(a)(3), label effective 20260819. It is one of 265 FDA drug label records sharing the active ingredient SALICYLIC ACID. 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 are most often described in connection with: wash affected, dry thoroughly, apply small, amount time, applicatorto sufficiently, wart let, twice daily, needed until. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Wash affected area and dry thoroughly.Apply a small amount at a time with the applicatorto sufficiently cover each wart. Let dry.Repeat once or twice daily as needed until thewart is removed,for up to 12 weeks
Dosage & Administration
Repeat once or twice daily as needed until thewart is removed, for up to 12 weeks.
Warnings
For external use only.
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View labelHow products containing SALICYLIC ACID compare
FDA lists 265 drug label records with SALICYLIC ACID 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 |
|---|---|---|---|
| — | — | L'Oreal USA Products Inc | 20 |
| — | — | Guangzhou Hechuang Commercial Service Co.,Ltd. | 8 |
| — | — | Kenvue Brands LLC | 6 |
| — | — | COSMETIQUE ACTIVE PRODUCTION | 5 |
| — | — | CVS Health | 5 |
Frequently asked questions
What is Txovis SKIN WART CORN REMOVER used for?
Wash affected area and dry thoroughly.Apply a small amount at a time with the applicatorto sufficiently cover each wart. Let dry.Repeat once or twice daily as needed until thewart is removed,for up to 12 weeks
Who makes Txovis SKIN WART CORN REMOVER?
Guangdong Joyan Biological Technology Co.,Ltd is the labeler of record for Txovis SKIN WART CORN REMOVER. 265 FDA label records share the active ingredient SALICYLIC ACID, 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 Txovis SKIN 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 Txovis SKIN 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?
Yes. 265 FDA drug label records list SALICYLIC ACID 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 Txovis SKIN 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.