AIADR Liquid WART CORN REMOVER

SALICYLIC ACID 17% LIQUID WART CORN REMOVER TOPICAL HUMAN OTC DRUG

AIADR Liquid WART CORN REMOVER is an FDA drug label for the active ingredient SALICYLIC ACID 17% LIQUID WART CORN REMOVER manufactured by Wenzhou Yuyuan Pharmaceutical 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 20260821.

Generic name
SALICYLIC ACID 17% LIQUID WART CORN REMOVER
Manufacturer
Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87786-043
Application
M028
Label effective
20260821

About this product

AIADR Liquid WART CORN REMOVER is an FDA-registered drug product whose active ingredient is SALICYLIC ACID 17% LIQUID WART CORN REMOVER. It is labelled by Wenzhou Yuyuan Pharmaceutical Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87786-043, application M028, label effective 20260821. It is one of 5 FDA drug label records sharing the active ingredient SALICYLIC ACID 17% LIQUID WART CORN REMOVER. 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 17% LIQUID WART CORN REMOVER are most often described in connection with: removal common, warts plantar. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Salicylic acid 17%

Indications & Usage

Uses For the removal of common warts, plantar warts, corns and calluses.

Dosage & Administration

Directions 1.Wash the affected area. Soak the wart in warm water for about 5 minutes(optional). 2.Pat the area dry thoroughly. 3.Using a cotton swab, apply enough liquid to completely cover each wart.A film will form over the wart within one minute. 4.Repeat once or twice daily as needed until the wart is removed, for up to 12 weeks.

Warnings

Warnings For external use only.

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How products containing SALICYLIC ACID 17% LIQUID WART CORN REMOVER compare

FDA lists 5 drug label records with SALICYLIC ACID 17% LIQUID WART CORN REMOVER 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 formProductsManufacturerProducts
— — Jiangxi Yudexi Pharmaceutical Co., LTD 4
— — Wenzhou Yuyuan Pharmaceutical Co., Ltd. 1
— — — —
— — — —
— — — —

Frequently asked questions

What is AIADR Liquid WART CORN REMOVER used for?
Uses For the removal of common warts, plantar warts, corns and calluses.

Who makes AIADR Liquid WART CORN REMOVER?
Wenzhou Yuyuan Pharmaceutical Co., Ltd. is the labeler of record for AIADR Liquid WART CORN REMOVER. 5 FDA label records share the active ingredient SALICYLIC ACID 17% LIQUID WART CORN REMOVER, 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 AIADR Liquid WART CORN 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 AIADR Liquid WART CORN 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 17% LIQUID WART CORN REMOVER?
Yes. 5 FDA drug label records list SALICYLIC ACID 17% LIQUID WART CORN REMOVER 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 AIADR Liquid WART CORN 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.