Aqua De Folli Hair Booster Pro
NDC Package 80592-201-01

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.

Aqua De Folli Hair Booster Pro is - ​Apply 1 vial once a week directly onto the scalp in the hair loss area- Continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again. Marketed by Rokit Healthcare Inc., this product is identified by NDC 80592-201.

Identification & Billing

NDC Package Code
80592-201-01
Package Description
3 mL in 1 BOTTLE
Product Code
80592-201
11-Digit Billing Format
80592020101

Clinical Specifications

Proprietary Name
Aqua De Folli Hair Booster Pro
Dosage Form
-
Usage Information
- ​Apply 1 vial once a week directly onto the scalp in the hair loss area- Continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again

Regulatory & Marketing

Labeler Name
Rokit Healthcare Inc.
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
09-24-2020
Listing Expiration
12-31-2021
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 80592-201-01 identifies a specific commercial package of 3 ml in 1 bottle of Aqua De Folli Hair Booster Pro, labeled by Rokit Healthcare Inc.. 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 Rokit Healthcare Inc. on September 24, 2020. The current certification is valid through December 31, 2021.

How is this Rokit Healthcare Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 80592020101. 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)
80592-201-01
11-Digit CMS (5-4-2)
80592-0201-01

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