Wart Remover Liquid
NDC Package 88064-123-01

11-digit billing NDC: 88064012301
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Wart Remover liquids is uses for the removal of common warts for the removal of plantar wartsDirections wash affected area; apply a thin layer; allow to dry; repeat once or twice daily; continue use up to 12 weeks. This formulation utilizes a liquid delivery system. Marketed by Shenzhen Baifanghui Technology Co., Ltd, this product is identified by NDC 88064-123.

Identification & Billing

NDC Package Code
88064-123-01
Package Description
5 BAG in 1 BOX / 1 LIQUID in 1 BAG
Product Code
88064-123
11-Digit Billing Format
88064012301

Clinical Specifications

Proprietary Name
Wart Remover
Non-Proprietary Name
Wart Remover
Substance Name
Salicylic Acid
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
SALICYLIC ACID .4 g/1
Usage Information
Uses for the removal of common warts for the removal of plantar wartsDirections wash affected area; apply a thin layer; allow to dry; repeat once or twice daily; continue use up to 12 weeks

Regulatory & Marketing

Labeler Name
Shenzhen Baifanghui Technology Co., Ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
10-09-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 88064-123-01 identifies a specific commercial package of 5 bag in 1 box / 1 liquid in 1 bag of Wart Remover, a human over the counter drug labeled by Shenzhen Baifanghui Technology Co., Ltd. This liquid is formulated for cutaneous use and contains salicylic acid as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Shenzhen Baifanghui Technology Co., Ltd on October 09, 2026. The current certification is valid through December 31, 2027.

How is this Shenzhen Baifanghui Technology Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 88064012301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
88064-123-01
11-Digit CMS (5-4-2)
88064-0123-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.