Nekvnro Acne Patch
NDC Package 84613-051-01

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.

Nekvnro Acne Patch is a medication used as Acne patch. Marketed by Shenzhen Xingqi Technology Co., Ltd., this product is identified by NDC 84613-051 and is authorized under FDA application M030.

Identification & Billing

NDC Package Code
84613-051-01
Package Description
30 g in 1 BOX
Product Code
84613-051
11-Digit Billing Format
84613005101

Clinical Specifications

Proprietary Name
Nekvnro Acne Patch
Dosage Form
-
Usage Information
This product is used as Acne patch. 1: Wipe dry after cleansing, Apply this product to the acne area. 2: The pimple will swell and turn white. 3: Wait for acne to gradually subside 4: Start from the edge and peel it off gently, Then take it down.

Regulatory & Marketing

Labeler Name
Shenzhen Xingqi Technology Co., Ltd.
FDA Application #
M030
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-08-2024
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 84613-051-01 identifies a specific commercial package of 30 g in 1 box of Nekvnro Acne Patch, labeled by Shenzhen Xingqi 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 Xingqi Technology Co., Ltd. on August 08, 2024. The current certification is valid through December 31, 2025.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84613005101. 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)
84613-051-01
11-Digit CMS (5-4-2)
84613-0051-01

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