Revox
NDC Package 72029-001-01

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.

Revox is to prevent DandruffPrevents potential scaly and dryness on scalp up to 100% through anti-irritation property. Marketed by Geomass Arastirma Gelistirme Enerji Petrol Maden Sis Ilac Ve Koz Urun Im San Tic Ltd Sti, this product is identified by NDC 72029-001 and is authorized under FDA application part358H.

Identification & Billing

NDC Package Code
72029-001-01
Package Description
1 BOTTLE in 1 CARTON / 400 mL in 1 BOTTLE
Product Code
72029-001
11-Digit Billing Format
72029000101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Revox
Dosage Form
-
Usage Information
To prevent DandruffPrevents potential scaly and dryness on scalp up to 100% through anti-irritation property.

Regulatory & Marketing

Labeler Name
Geomass Arastirma Gelistirme Enerji Petrol Maden Sis Ilac Ve Koz Urun Im San Tic Ltd Sti
FDA Application #
part358H
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-30-2018
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 72029-001-01 identifies a specific commercial package of 1 bottle in 1 carton / 400 ml in 1 bottle of Revox, labeled by Geomass Arastirma Gelistirme Enerji Petrol Maden Sis Ilac Ve Koz Urun Im San Tic Ltd Sti. 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 Geomass Arastirma Gelistirme Enerji Petrol Maden Sis Ilac Ve Koz Urun Im San Tic Ltd Sti on January 30, 2018. The current certification is valid through December 31, 2021.

How is this Geomass Arastirma Gelistirme Enerji Petrol Maden Sis Ilac Ve Koz Urun Im San Tic Ltd Sti product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72029000101. 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)
72029-001-01
11-Digit CMS (5-4-2)
72029-0001-01

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