MEOLY Wart Remover Pads 40 g/1001

Wart Remover Pads · PATCH · Shenzhen Xinxin Yunhai Technology Co., Ltd.

No Recall History

Plain English

MEOLY Wart Remover Pads is a patch containing wart remover pads at 40 g/1001, taken topical. Manufactured by Shenzhen Xinxin Yunhai Technology Co., Ltd..

Key Facts

Brand Name: MEOLY Wart Remover Pads
Generic Name: Wart Remover Pads
NDC Code (Product): 83818-010
Manufacturer: Shenzhen Xinxin Yunhai Technology Co., Ltd.
Strength: 40 g/1001
Dosage Form: PATCH
Route: TOPICAL
Marketing Status
Application #: M028
Marketing Start: 02/17/2025

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Use For the effective removal of warts.

Dosage & Administration

Directions Not for use on children under 12 years withoutdoctor's advice.Avoid contact with healthy skin; protect surroundingskin with Vaseline. For external use only. Discontinue use if irritation occurs. Keep out of reach of children. Store in a cool, dry place.

Warnings

Warnings Not for use on children under 12 years withoutdoctor's advice. Avoid contact with healthy skin; protect surroundingskin with Vaseline. For external use only. Discontinue use if irritation occurs. Keep out of reach of children. Store in a cool, dry place.

Frequently Asked Questions

What is MEOLY Wart Remover Pads used for?

MEOLY Wart Remover Pads contains Wart Remover Pads. It is a patch taken topical. Consult your doctor for specific uses.

Is MEOLY Wart Remover Pads a controlled substance?

MEOLY Wart Remover Pads is not classified as a controlled substance by the DEA.

What is the generic name for MEOLY Wart Remover Pads?

The generic name for MEOLY Wart Remover Pads is Wart Remover Pads. There are no other listed brand versions of Wart Remover Pads.

What is the NDC code for MEOLY Wart Remover Pads 40 g/1001?

The NDC (National Drug Code) for MEOLY Wart Remover Pads 40 g/1001 is 83818-010, listed by Shenzhen Xinxin Yunhai Technology Co., Ltd..

Product NDC

83818-010

Package NDC

83818-010-01

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

Data from openFDA · Public domain (CC0 1.0)