Genital wart removal onitment
Genital wart removal onitment is an FDA drug label for the active ingredient SALICYLIC ACID 40% manufactured by Guangxi Keyun E-commerce 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 20260416.
- Generic name
- SALICYLIC ACID 40%
- Manufacturer
- Guangxi Keyun E-commerce Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87278-011
- Application
- M026
- Label effective
- 20260416
About this product
Genital wart removal onitment is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 40%. It is labelled by Guangxi Keyun E-commerce Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87278-011, application M026, label effective 20260416. It is one of 33 FDA drug label records sharing the active ingredient SALICYLIC ACID 40%. 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% are most often described in connection with: removal common, wart easily, rough cauliflower-like. 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 common warts. The common wart is easily recognized by the rough"cauliflower-like" appear-ance of the surface.
Dosage & Administration
Wash affected area (may soak wart in warm water for 5 minutes if desired) Dry area thoroughly. Apply small amount by hand to covereach wart. Let dry. Repeat this procedure twice dailyas needed for up to 12 weeks
Warnings
For external use only If the product gets into eyes, flush with water for 15 minutes. Avoid inhaling vapours.
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View labelHow products containing SALICYLIC ACID 40% compare
FDA lists 33 drug label records with SALICYLIC ACID 40% 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 |
|---|---|---|---|
| — | — | Guangzhou Huixue Biotechnology Co., Ltd. | 14 |
| — | — | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 12 |
| — | — | Jiangxi Yudexi Pharmaceutical Co., LTD | 4 |
| — | — | Guangxi Keyun E-commerce Co., Ltd. | 1 |
| — | — | Guangzhou Chuanglian Zhida Trading Co., Ltd | 1 |
Frequently asked questions
What is Genital wart removal onitment used for?
Use For the removal of common warts. The common wart is easily recognized by the rough"cauliflower-like" appear-ance of the surface.
Who makes Genital wart removal onitment?
Guangxi Keyun E-commerce Co., Ltd. is the labeler of record for Genital wart removal onitment. 33 FDA label records share the active ingredient SALICYLIC ACID 40%, 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 Genital wart removal onitment 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 Genital wart removal onitment 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%?
Yes. 33 FDA drug label records list SALICYLIC ACID 40% 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 Genital wart removal onitment 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.