Wart Remover Liquid
Wart Remover Liquid is an FDA drug label for the active ingredient WART REMOVER LIQUID manufactured by Shenzhen Earth Surface Trading 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 20260927.
- Generic name
- WART REMOVER LIQUID
- Manufacturer
- Shenzhen Earth Surface Trading Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85636-005
- Application
- M028
- Label effective
- 20260927
About this product
Wart Remover Liquid is an FDA-registered drug product whose active ingredient is WART REMOVER LIQUID. It is labelled by Shenzhen Earth Surface Trading Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85636-005, application M028, label effective 20260927. It is one of 4 FDA drug label records sharing the active ingredient WART REMOVER LIQUID. 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 WART REMOVER LIQUID are most often described in connection with: removal common, plantar warts, wart easily, rough cauliflower-like, location only, footprint pattern. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Uses · for the removal of common and plantar warts · the common wart is easily recognized by the rough”cauliflower-like” appearance of the surface · the plantar wart is recognized by its location only on the bottom of the foot,its tenderness and the interruption of the footprint pattern
Warnings
Warnings For external use only. keep away from fire and flame. only use on affected area.
More products with the same ingredient
WART REMOVER LIQUIDHow products containing WART REMOVER LIQUID compare
FDA lists 4 drug label records with WART REMOVER LIQUID 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 |
|---|---|---|---|
| — | — | CVS Pharmacy | 1 |
| — | — | Guangzhou Yilong Cosmetics.,Ltd | 1 |
| — | — | Perrigo Direct, Inc | 1 |
| — | — | Shenzhen Earth Surface Trading Co., Ltd. | 1 |
| — | — | — | — |
Frequently asked questions
What is Wart Remover Liquid used for?
Uses Uses · for the removal of common and plantar warts · the common wart is easily recognized by the rough”cauliflower-like” appearance of the surface · the plantar wart is recognized by its location only on the bottom of the foot,its tenderness and the interruption of the footprint pattern
Who makes Wart Remover Liquid?
Shenzhen Earth Surface Trading Co., Ltd. is the labeler of record for Wart Remover Liquid. 4 FDA label records share the active ingredient WART REMOVER LIQUID, 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 Wart Remover Liquid 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 Wart Remover Liquid 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 WART REMOVER LIQUID?
Yes. 4 FDA drug label records list WART REMOVER LIQUID 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 Wart Remover Liquid 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.