Sefudun Nail Fungus Treatment Liquid
NDC Package 83804-002-01
Package Information
Sefudun Nail Fungus Treatment (zingiber officinale (ginger) root extract) liquids is sEFUDUN 7-Day Nail Fungus Treatment is designed to repair and strengthen nails and cuticles, promoting healthier and stronger nails for both handsand feet. This formulation utilizes a liquid delivery system. Marketed by Shenzhen Shandian Jingling Technology Co., Ltd., this product is identified by NDC 83804-002 and is authorized under FDA application 505G(a)(3).
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 83804 - Shenzhen Shandian Jingling Technology Co., Ltd.
- 83804-002 - Sefudun Nail Fungus Treatment
- 83804-002-01 - 60 mL in 1 BOTTLE
- 83804-002 - Sefudun Nail Fungus Treatment
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 83804-002-01 identifies a specific commercial package of 60 ml in 1 bottle of Sefudun Nail Fungus Treatment, a human over the counter drug labeled by Shenzhen Shandian Jingling Technology Co., Ltd.. This liquid is formulated for topical use and contains ginger 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 Shandian Jingling Technology Co., Ltd. on May 09, 2025. The current certification is valid through December 31, 2026.
How is this Shenzhen Shandian Jingling Technology Co., Ltd. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 83804000201. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.