Wart Remove
NDC Package 84322-002-01

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 Remove is 1. Marketed by Shenzhen Gaoye E-commerce Co., Ltd, this product is identified by NDC 84322-002 and is authorized under FDA application M028.

Identification & Billing

NDC Package Code
84322-002-01
Package Description
15 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
84322000201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Wart Remove
Dosage Form
-
Usage Information
1. Wash the corns or warts with warm water. 2. Take out the inner plug from the bottle, install the brush into the bottle cap. press the brush tightly, and tighten the cap on the bottle. 3. Dry the skin, then open the cap, dip the brush into the liquid with the brush and apply it to the wart or corn,after the liquid dries and forms a mask, apply the liquid again. 4. Repeat this procedure once or twice daily as needed (until the wart is removed) for up to 12 weeks.

Regulatory & Marketing

Labeler Name
Shenzhen Gaoye E-commerce Co., Ltd
FDA Application #
M028
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-13-2024
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 84322-002-01 identifies a specific commercial package of 15 ml in 1 bottle of Wart Remove, labeled by Shenzhen Gaoye E-commerce 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 Gaoye E-commerce Co., Ltd on May 13, 2024. The current certification is valid through December 31, 2025.

How is this Shenzhen Gaoye E-commerce Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84322000201. 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)
84322-002-01
11-Digit CMS (5-4-2)
84322-0002-01

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