Dizop Minoxidil Topical Gel
NDC Package 83766-102-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Dizop Minoxidil Topical Gel is apply 3-4 drops of Minoxidil Gel directly to the scalp in the area to be treated. Marketed by Shenzhen Joyuflsh Technology Co.,ltd., this product is identified by NDC 83766-102.

Identification & Billing

NDC Package Code
83766-102-01
Package Description
2 CANISTER in 1 PACKAGE / 60 g in 1 CANISTER
Product Code
83766-102
11-Digit Billing Format
83766010201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dizop Minoxidil Topical Gel
Dosage Form
-
Usage Information
Apply 3-4 drops of Minoxidil Gel directly to the scalp in the area to be treated. Massage into the scalp with your fingers then wash hands thoroughly. Using more or using more often will not improve results; continued use is necessary to promote and maintain hair regrowth.

Regulatory & Marketing

Labeler Name
Shenzhen Joyuflsh Technology Co.,ltd.
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
10-26-2023
End Marketing Date
10-31-2023
Listing Expiration
10-31-2023
Exclude Flag
D
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (83766-102). Click a package code to view its specific billing and regulatory data.

83766-102-02
1 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE (83766-102-01)
83766-102-02
3 CANISTER in 1 PACKAGE / 60 g in 1 CANISTER
83766-102-04
1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE (83766-102-03)

* 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 83766-102-01 identifies a specific commercial package of 2 canister in 1 package / 60 g in 1 canister 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 October 31, 2023.

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: 83766010201. 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)
83766-102-01
11-Digit CMS (5-4-2)
83766-0102-01

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