Supreh Bee Venom Skin Tag Treatment Liquid
NDC Package 83818-012-01

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 Skin Tag Treatment Liquid (supreh bee venom skin tag remover liquid) liquids is adult s & children 4 years and over: Wash hands before & after use. This formulation utilizes a liquid delivery system. Marketed by Shenzhen Xinxin Yunhai Technology Co., Ltd., this product is identified by NDC 83818-012 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
83818-012-01
Package Description
30 mL in 1 BOTTLE
Product Code
83818-012
11-Digit Billing Format
83818001201

Clinical Specifications

Proprietary Name
Supreh Bee Venom Skin Tag Treatment Liquid
Non-Proprietary Name
Supreh Bee Venom Skin Tag Remover Liquid
Substance Name
Apis Mellifera Venom; Calendula Officinalis Flower; Thuja Occidentalis Whole
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
Adult s & children 4 years and over: Wash hands before & after use. Shake well& apply 1 or 2 drops to a cotton swab and dab directly to the tags 3 times daily. Do not oversaturate or exceed dosage. It is important not to miss applications. Children under 4 yrs: Do not use

Regulatory & Marketing

Labeler Name
Shenzhen Xinxin Yunhai Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-23-2025
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 83818-012-01 identifies a specific commercial package of 30 ml in 1 bottle of Supreh Bee Venom Skin Tag Treatment Liquid, 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; calendula officinalis flower; thuja occidentalis whole 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 May 23, 2025. 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: 83818001201. 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)
83818-012-01
11-Digit CMS (5-4-2)
83818-0012-01

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