TepidSun WART REMOVER

TepidSun WART REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 40%. It is labelled by Guangzhou Huixue Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87204-202, application M028, label effective 20260908. 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.

Across FDA labelling, products containing SALICYLIC ACID 40% are most often described in connection with: affected area, removal warts, calluses clean, warm water, minutes optional, take appropriate, making sure, covers completely. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

For the removal of warts, including warts, corns, and calluses.1.Clean the affected area, You can soak the affected area in warm water for 5 minutes (optional). 2. Take an appropriate amount of the solution and apply it to the affected area, making sure it covers completely. Wait for it to dry 3. Repeat this process 2-3 times daily until the skin looks smooth. More severe may recuire more time Patience and perseverance are required during its use. The longest continuous use period is no more than 12 weeks.

1Clean the affected area. You can soak the affected area in warm water for 5 minutes (optional). 2. Take an appropriate amount of the solution and apply it to the affected area, making sure it covers completely. Wait for it to dry. 3. Repeat this process 2-3 times daily until the skin looks smooth.

. For external use only. • Flammable Keep away from fire and flame. .Keep out of reach of children, .Avoid contact with eyes, in case of contact, flush eyes with plenty of cool water. . Do not swallow, if swallowed, seek medical attention or contact a Poison Control Center (1-800-222-1222) immediately.• Children should use this product under adult supervision. .Avoid prolonged exposure to air during use as the substance may dissolve and crystallize easily. . Recap immediately after each use. Do not use if the cap is broken or missing.

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.

What is TepidSun WART REMOVER used for?
For the removal of warts, including warts, corns, and calluses.1.Clean the affected area, You can soak the affected area in warm water for 5 minutes (optional). 2. Take an appropriate amount of the solution and apply it to the affected area, making sure it covers completely. Wait for it to dry 3. Repeat this process 2-3 times daily until the skin looks smooth. More severe may recuire more time …

Who makes TepidSun WART REMOVER?
Guangzhou Huixue Biotechnology Co., Ltd. is the labeler of record for TepidSun WART REMOVER. 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 TepidSun WART 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 TepidSun WART 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 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 TepidSun WART 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.