WARTREMOVERLIQUID
WARTREMOVERLIQUID is an FDA drug label for the active ingredient WARTREMOVER manufactured by Shenzhen yuehaotong 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 20260627.
- Generic name
- WARTREMOVER
- Manufacturer
- Shenzhen yuehaotong Technology Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87492-004
- Application
- M028
- Label effective
- 20260627
About this product
WARTREMOVERLIQUID is an FDA-registered drug product whose active ingredient is WARTREMOVER. It is labelled by Shenzhen yuehaotong Technology Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87492-004, application M028, label effective 20260627. 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 WARTREMOVER are most often described in connection with: plantar warts, removal commonwarts, rough cauliflower-like, surface andare, easily recognizable, located onlyon, feet tenderto, interruptedfootprint pattern. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
Uses For the removal of commonwarts and plantar warts.Common warts have a rough"cauliflower-like" surface andare easily recognizable.Plantar warts are located onlyon the soles of the feet, tenderto touch, with an interruptedfootprint pattern.
Dosage & Administration
Dosage and administration For external use only.
Warnings
Warnings For external use only. Flammable: Keep away from fire or flame
Frequently asked questions
What is WARTREMOVERLIQUID used for?
Uses For the removal of commonwarts and plantar warts.Common warts have a rough"cauliflower-like" surface andare easily recognizable.Plantar warts are located onlyon the soles of the feet, tenderto touch, with an interruptedfootprint pattern.
Who makes WARTREMOVERLIQUID?
Shenzhen yuehaotong Technology Co., Ltd is the labeler of record for WARTREMOVERLIQUID.
What form does WARTREMOVERLIQUID 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 WARTREMOVERLIQUID 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.
Has WARTREMOVERLIQUID 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.