Quick-acting Wart Removal
NDC Package 83575-001-01

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 inactivated by the FDA.

Quick-acting Wart Removal is -Wash the affffected area by soaking the wart in warm water for 5 minutes - Dry thoroughly,apply one drop at a time with applicator to suffiffifficiently cover each wart - Let it dry, self-adhesive masking sheets can be used to hide warts - 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 83575-001 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
83575-001-01
Package Description
30 mL in 1 BOX
Product Code
83575-001
11-Digit Billing Format
83575000101

Clinical Specifications

Proprietary Name
Quick-acting Wart Removal
Dosage Form
-
Usage Information
-Wash the affffected area by soaking the wart in warm water for 5 minutes - Dry thoroughly,apply one drop at a time with applicator to suffiffifficiently cover each wart - Let it dry, self-adhesive masking sheets can be used to hide warts - 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-12-2023
Listing Expiration
12-31-2024
Exclude Flag
I
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 83575-001-01 identifies a specific commercial package of 30 ml in 1 box of Quick-acting 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 July 12, 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: 83575000101. 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)
83575-001-01
11-Digit CMS (5-4-2)
83575-0001-01

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