Dizop Minoxidil Topical Gel
NDC Package 83766-101-02

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Dizop Minoxidil Topical Gel is hair regrowth treatment for men. Marketed by Shenzhen Joyuflsh Technology Co.,ltd., this product is identified by NDC 83766-101 and is authorized under FDA application M032.

Identification & Billing

NDC Package Code
83766-101-02
Package Description
1 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE (83766-101-01)
Product Code
83766-101
11-Digit Billing Format
83766010102
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dizop Minoxidil Topical Gel
Dosage Form
-
Usage Information
Hair regrowth treatment for men. Use to Regrow Hair on the Top of the Scalp (See Pictures on the Side of this Carton).

Regulatory & Marketing

Labeler Name
Shenzhen Joyuflsh Technology Co.,ltd.
FDA Application #
M032
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-26-2023
Listing Expiration
12-31-2025
Exclude Flag
I
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 83766-101-02 identifies a specific commercial package of 1 bottle in 1 carton / 100 ml in 1 bottle (83766-101-01) of Dizop Minoxidil Topical Gel, labeled by Shenzhen Joyuflsh 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 Joyuflsh Technology Co.,ltd. on October 26, 2023. The current certification is valid through December 31, 2025.

How is this Shenzhen Joyuflsh Technology Co.,ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83766010102. 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)
83766-101-02
11-Digit CMS (5-4-2)
83766-0101-02

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