Mqforu Pain Patch
NDC Package 83781-010-06

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

Package Information

Mqforu Pain Patch (pain patch) patches is adults and children over 12 years:■clean and dry the affected area■remove backing from patch and apply patch to affected area■use 1 patch per knee for 8 to 12 hours, once per day children 12 years or younger: ask a doctor. This formulation utilizes a patch delivery system. Marketed by Zhengzhou Miaoqi Medical Technology Co., Ltd., this product is identified by NDC 83781-010 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
83781-010-06
Package Description
60 PATCH in 1 BOX
Product Code
11-Digit Billing Format
83781001006

Clinical Specifications

Proprietary Name
Mqforu Pain Patch
Non-Proprietary Name
Pain Patch
Substance Name
Borneol; Camphor (synthetic); Menthol
Dosage Form
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Usage Information
Adults and children over 12 years:■clean and dry the affected area■remove backing from patch and apply patch to affected area■use 1 patch per knee for 8 to 12 hours, once per day children 12 years or younger: ask a doctor

Regulatory & Marketing

Labeler Name
Zhengzhou Miaoqi Medical Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-13-2024
Listing Expiration
12-31-2026
Exclude Flag
N
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 (83781-010). Click a package code to view its specific billing and regulatory data.

10 PATCH in 1 BOX
20 PATCH in 1 BOX
30 PATCH in 1 BOX
40 PATCH in 1 BOX
50 PATCH in 1 BOX
100 PATCH 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 83781-010-06 identifies a specific commercial package of 60 patch in 1 box of Mqforu Pain Patch, a human over the counter drug labeled by Zhengzhou Miaoqi Medical Technology Co., Ltd.. This patch is formulated for topical use and contains borneol; camphor (synthetic); menthol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Zhengzhou Miaoqi Medical Technology Co., Ltd. on August 13, 2024. The current certification is valid through December 31, 2026.

How is this Zhengzhou Miaoqi Medical Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83781001006. 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)
83781-010-06
11-Digit CMS (5-4-2)
83781-0010-06

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