Wart Removal
NDC Package 83575-003-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Wart Removal is - a wash affected area , may soak wart in warmwater for 5 minuteso- dry thoroughly, apply one drop at a time withapplicator to sufficiently cover each wart- let dry , self-adhesive cover-up discs may beused to conceal wart - Repeat procedure once or twice daily as needed (until wart is removed) for up to 12 weeks. Marketed by Shenzhenshi Liuxiang Yuntian Network Technology Co., Ltd., this product is identified by NDC 83575-003 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
83575-003-01
Package Description
50 g in 1 BOX
Product Code
11-Digit Billing Format
83575000301
RxNorm Crosswalk
  • RxCUI: 2668431 - chlorhexidine acetate 0.3 % / salicylic acid 15 % Topical Ointment
  • RxCUI: 2668431 - chlorhexidine acetate 0.003 MG/MG / salicylic acid 0.15 MG/MG Topical Ointment

Clinical Specifications

Proprietary Name
Wart Removal
Dosage Form
-
Usage Information
- a wash affected area , may soak wart in warmwater for 5 minuteso- dry thoroughly, apply one drop at a time withapplicator to sufficiently cover each wart- let dry , self-adhesive cover-up discs may beused to conceal wart - Repeat procedure once or twice daily as needed (until wart is removed) for up to 12 weeks

Regulatory & Marketing

Labeler Name
Shenzhenshi Liuxiang Yuntian Network Technology Co., Ltd.
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-30-2023
Listing Expiration
12-31-2024
Exclude Flag
I
Sample Package
No

Hierarchy Structure

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (83575-003). Click a package code to view its specific billing and regulatory data.

50 g in 1 BOX

* 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 83575-003-01 identifies a specific commercial package of 50 g in 1 box of Wart Removal, labeled by Shenzhenshi Liuxiang Yuntian Network 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 Shenzhenshi Liuxiang Yuntian Network Technology Co., Ltd. on October 30, 2023. The current certification is valid through December 31, 2024.

How is this Shenzhenshi Liuxiang Yuntian Network Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83575000301. 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)
83575-003-01
11-Digit CMS (5-4-2)
83575-0003-01

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