Supreh Bee Venom Wart Corn Treatment Liquid
NDC Package 83818-005-01

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

Package Information

Supreh Bee Venom Wart Corn Treatment (bee venom wart corn treatment) liquids is 1.Clean and dry the area. This formulation utilizes a liquid delivery system. Marketed by Shenzhen Xinxin Yunhai Technology Co., Ltd., this product is identified by NDC 83818-005 and is authorized under FDA application M028.

Identification & Billing

NDC Package Code
83818-005-01
Package Description
20 mL in 1 BOTTLE
Product Code
83818-005
11-Digit Billing Format
83818000501

Clinical Specifications

Proprietary Name
Supreh Bee Venom Wart Corn Treatment
Non-Proprietary Name
Bee Venom Wart Corn Treatment
Substance Name
Apis Mellifera Venom; 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.Clean and dry the area. 2.Open, attach brush, dip, and apply. Reapply when dry. 3.For feet, use at night to reduce friction. 4.Use daily for at least 2 weeks, longer for severe cases.

Regulatory & Marketing

Labeler Name
Shenzhen Xinxin Yunhai Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M028
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-25-2024
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 83818-005-01 identifies a specific commercial package of 20 ml in 1 bottle of Supreh Bee Venom Wart Corn Treatment, a human over the counter drug labeled by Shenzhen Xinxin Yunhai Technology Co., Ltd.. This liquid is formulated for topical use and contains apis mellifera venom; 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 Shenzhen Xinxin Yunhai Technology Co., Ltd. on October 25, 2024. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83818000501. 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)
83818-005-01
11-Digit CMS (5-4-2)
83818-0005-01

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