QKEKL WART REMOVER

SALICYLIC ACID 45% TOPICAL HUMAN OTC DRUG

QKEKL WART REMOVER is an FDA drug label for the active ingredient SALICYLIC ACID 45% manufactured by Guangzhou Huixue Biotechnology 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 20260907.

Generic name
SALICYLIC ACID 45%
Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87204-212
Application
M028
Label effective
20260907

About this product

QKEKL WART REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 45%. It is labelled by Guangzhou Huixue Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87204-212, application M028, label effective 20260907. 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 45% are most often described in connection with: affected area, removal warts, includinn nlantar, calluses clean, warm water, minutes optional, take appropriate, making sure. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Salicylic Acid 45%

Indications & Usage

For the removal of warts includinn nlantar warts flat warts common 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 complete ly. Wait for it to dry. 3. Repeat this process 2-3 times daily until the skin looks smooth 4. More severe may require more time.Patience and perseverance are required during its use. The longest continuous use period is no more than 12 weeks.

Dosage & Administration

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.

Warnings

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 c cool water. .Do not swallow, if swallowed, seek medical attention or contact a Poisor 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.

Frequently asked questions

What is QKEKL WART REMOVER used for?
For the removal of warts includinn nlantar warts flat warts common 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 complete ly. Wait for it to dry. 3. Repeat this process 2-3 times daily until the skin looks smooth 4. …

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

What form does QKEKL 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 QKEKL 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.

Has QKEKL 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.

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.