Fymiox Minoxidil Hair Growth Spray.
NDC Package 84213-001-01
Package Information
Fymiox Minoxidil Hair Growth Spray. is use the spray head to apply the serum to the scalp in the area of thinning Please do an allergy test before use. Marketed by Shenzhen Weilaiwang Technology Co., Ltd, this product is identified by NDC 84213-001 and is authorized under FDA application M032.
Identification & Billing
- RxCUI: 1537948 - minoxidil 5 % Topical Spray
- RxCUI: 1537948 - minoxidil 50 MG/ML Topical Spray
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 84213 - Shenzhen Weilaiwang Technology Co., Ltd
- 84213-001 - Fymiox Minoxidil Hair Growth Spray.
- 84213-001-01 - 50 mL in 1 BOTTLE
- 84213-001 - Fymiox Minoxidil Hair Growth Spray.
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 (84213-001). Click a package code to view its specific billing and regulatory data.
* 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 84213-001-01 identifies a specific commercial package of 50 ml in 1 bottle of Fymiox Minoxidil Hair Growth Spray., labeled by Shenzhen Weilaiwang Technology Co., Ltd. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Shenzhen Weilaiwang Technology Co., Ltd on March 28, 2024. The current certification is valid through December 31, 2025.
How is this Shenzhen Weilaiwang Technology Co., Ltd product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 84213000101. 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.