KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS
KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS is an FDA drug label for the active ingredient WART REMOVER FOR COMMON PLANTAR WARTS manufactured by Shenzhen Xituo Electronics 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 20260525.
- Generic name
- WART REMOVER FOR COMMON PLANTAR WARTS
- Manufacturer
- Shenzhen Xituo Electronics Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87273-003
- Application
- M028
- Label effective
- 20260525
About this product
KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS is an FDA-registered drug product whose active ingredient is WART REMOVER FOR COMMON PLANTAR WARTS. It is labelled by Shenzhen Xituo Electronics Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87273-003, application M028, label effective 20260525. It is one of 2 FDA drug label records sharing the active ingredient WART REMOVER FOR COMMON PLANTAR WARTS. 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 FOR COMMON PLANTAR WARTS are most often described in connection with: removal ofcommon, plantar 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 ofcommon and plantar warts
Dosage & Administration
Directions wash affected area may soak wart in warm water for 5 minutes dry area thoroughly using the applicator, apply one drop at a time to sufficiently cover each wart let dry repeat this procedure once or twice daily as needed (until wart is removed) treatment may take up to 12 weeks
Warnings
Warnings for external use only
More products with the same ingredient
WART REMOVER FOR COMMON PLANTAR WARTSHow products containing WART REMOVER FOR COMMON PLANTAR WARTS compare
FDA lists 2 drug label records with WART REMOVER FOR COMMON PLANTAR WARTS 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 |
|---|---|---|---|
| — | — | Shenzhen Xituo Electronics Co., Ltd | 2 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS used for?
Use for the removal ofcommon and plantar warts
Who makes KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS?
Shenzhen Xituo Electronics Co., Ltd is the labeler of record for KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS. 2 FDA label records share the active ingredient WART REMOVER FOR COMMON PLANTAR WARTS, 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 KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS 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 KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS 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 FOR COMMON PLANTAR WARTS?
Yes. 2 FDA drug label records list WART REMOVER FOR COMMON PLANTAR WARTS 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 KTLEPOWER WART REMOVER FOR COMMON PLANTAR WARTS 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.