Wart Remover
NDC Package 84510-123-02

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 Remover is 1. Marketed by Binzhoutengfenshangmaoyouxiangongsi, this product is identified by NDC 84510-123.

Identification & Billing

NDC Package Code
84510-123-02
Package Description
1 BOTTLE in 1 BOX, UNIT-DOSE / 30 mL in 1 BOTTLE (84510-123-01)
Product Code
11-Digit Billing Format
84510012302

Clinical Specifications

Proprietary Name
Wart Remover
Dosage Form
-
Usage Information
1. Clean the skin before use, then wipe dry.2. Shake this product well before use, use a smudge brush to take 1-2 drops of makeup remover and apply it on the miliary skin, let it fully absorb and dry completely(Recommended to use twice a day until milia go away, which usually falls off within 7-14 days.)

Regulatory & Marketing

Labeler Name
Binzhoutengfenshangmaoyouxiangongsi
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
07-03-2024
Listing Expiration
12-31-2025
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 84510-123-02 identifies a specific commercial package of 1 bottle in 1 box, unit-dose / 30 ml in 1 bottle (84510-123-01) of Wart Remover, labeled by Binzhoutengfenshangmaoyouxiangongsi. 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 Binzhoutengfenshangmaoyouxiangongsi on July 03, 2024. The current certification is valid through December 31, 2025.

How is this Binzhoutengfenshangmaoyouxiangongsi product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84510012302. 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)
84510-123-02
11-Digit CMS (5-4-2)
84510-0123-02

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