Mqxunmi Bee Venom Corn Callus Removers Liquid
NDC Package 83781-013-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Mqxunmi Bee Venom Corn Callus Removers (bee venom corn callus removers) liquids is 1.Wash the corn & callus area with water and dry the skin. This formulation utilizes a liquid delivery system. Marketed by Zhengzhou Miaoqi Medical Technology Co., Ltd., this product is identified by NDC 83781-013 and is authorized under FDA application M030.

Identification & Billing

NDC Package Code
83781-013-01
Package Description
15 mL in 1 BOTTLE
Product Code
83781-013
11-Digit Billing Format
83781001301

Clinical Specifications

Proprietary Name
Mqxunmi Bee Venom Corn Callus Removers
Non-Proprietary Name
Bee Venom Corn Callus Removers
Substance Name
Apis Mellifera Venom; Honey; Salicylic Acid
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Active Ingredient(s)
Usage Information
1.Wash the corn & callus area with water and dry the skin. 2.Unscrew the cap to open. Dip the liquid with the brush and apply it on the affected area. Wait in minutes after the liquid dries and turn to mask and apply one more time. 3.Repeat the above process twice a day, morning and evening. If the issue is foot - based, apply before bedtime to minimize friction. 4.Continue daily application for at least 2 weeks until the skin appears smooth. More severe cases may require more time. Remain patient and consistent during the application.

Regulatory & Marketing

Labeler Name
Zhengzhou Miaoqi Medical Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M030
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-20-2025
Listing Expiration
12-31-2026
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (83781-013). Click a package code to view its specific billing and regulatory data.

83781-013-02
20 mL in 1 BOTTLE
83781-013-03
30 mL in 1 BOTTLE

* 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 83781-013-01 identifies a specific commercial package of 15 ml in 1 bottle of Mqxunmi Bee Venom Corn Callus Removers, a human over the counter drug labeled by Zhengzhou Miaoqi Medical Technology Co., Ltd.. This liquid is formulated for topical use and contains apis mellifera venom; honey; salicylic acid 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 October 20, 2025. 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: 83781001301. 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)
83781-013-01
11-Digit CMS (5-4-2)
83781-0013-01

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