Wart Remover
NDC Package 87276-261-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Wart Remover is wash the affected area May soak the wart in warm water for 5 minutes. Marketed by Shenzhen Zhenshangzekai Technology Co., Ltd., this product is identified by NDC 87276-261 and is authorized under FDA application M028.

Identification & Billing

NDC Package Code
87276-261-01
Package Description
1 g in 1 TUBE
Product Code
87276-261
11-Digit Billing Format
87276026101

Clinical Specifications

Proprietary Name
Wart Remover
Dosage Form
-
Usage Information
Wash the affected area May soak the wart in warm water for 5 minutes. Dry area thoroughly. Using the applicator, coat the wart with a thin layer of ointment to sufficiently covereach wart. Allow it to fully absorb and cover it with a bandage as needed.Repeat this procedure once or twice daily as needed (until the wart is removed) forup to 12 weeks.

Regulatory & Marketing

Labeler Name
Shenzhen Zhenshangzekai Technology Co., Ltd.
FDA Application #
M028
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-04-2026
End Marketing Date
08-06-2026
Listing Expiration
08-06-2026
Exclude Flag
D
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 87276-261-01 identifies a specific commercial package of 1 g in 1 tube of Wart Remover, labeled by Shenzhen Zhenshangzekai Technology Co., Ltd.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Shenzhen Zhenshangzekai Technology Co., Ltd. on February 04, 2026. The current certification is valid through August 06, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87276026101. 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)
87276-261-01
11-Digit CMS (5-4-2)
87276-0261-01

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