Drugplain

HEALMUSZ WART REMOVER 10 g/100g

Salicylic acid 10% WART REMOVER · LIQUID · Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.

No Recall History
Plain English

HEALMUSZ WART REMOVER is a liquid containing salicylic acid 10% wart remover at 10 g/100g, taken topical. Manufactured by Jiangxi Zhongletang Pharmaceuticals Co.,Ltd..

Key Facts

Brand Name
HEALMUSZ WART REMOVER
Generic Name
Salicylic acid 10% WART REMOVER
NDC Code (Product)
87686-002
Manufacturer
Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.
Strength
10 g/100g
Dosage Form
LIQUID
Route
TOPICAL
Marketing Status
Application #
M028
Marketing Start
05/12/2026

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Use ·for the removal of common and plantar warts ·the common wart is easily recognized by the rough “cauliflower-like” appearance on the surface.·the plantar wart is recognized by its location only on the bottom of the foot, its tenderness and interruption of the footprint pattern

Dosage & Administration

Directions wash affected area·may soak wart in warm water for 5 minutes· Use a cotton swab to apply a sufficient amount to cover each wart. Let it dry.repeat this procedure once or twice daily as needed (until wart is removed)for up to 12 weeks

Warnings

Warnings For external use only.

Frequently Asked Questions

What is HEALMUSZ WART REMOVER used for?

HEALMUSZ WART REMOVER contains Salicylic acid 10% WART REMOVER. It is a liquid taken topical. Consult your doctor for specific uses.

Is HEALMUSZ WART REMOVER a controlled substance?

HEALMUSZ WART REMOVER is not classified as a controlled substance by the DEA.

What is the generic name for HEALMUSZ WART REMOVER?

The generic name for HEALMUSZ WART REMOVER is Salicylic acid 10% WART REMOVER. There are no other listed brand versions of Salicylic acid 10% WART REMOVER.

What is the NDC code for HEALMUSZ WART REMOVER 10 g/100g?

The NDC (National Drug Code) for HEALMUSZ WART REMOVER 10 g/100g is 87686-002, listed by Jiangxi Zhongletang Pharmaceuticals Co.,Ltd..

Product NDC

87686-002

Package NDC

87686-002-01

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)