Gillette Endurance Ultimate Fresh Clear
NDC Package 69423-080-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Gillette Endurance Ultimate Fresh Clear is a . Marketed by Procter And Gamble Manufacturing Company, this product is identified by NDC 69423-080 and is authorized under FDA application part350.

Identification & Billing

NDC Package Code
69423-080-10
Package Description
107 g in 1 CYLINDER
Product Code
11-Digit Billing Format
69423008010

Clinical Specifications

Proprietary Name
Gillette Endurance Ultimate Fresh Clear
Dosage Form
-

Regulatory & Marketing

Labeler Name
Procter And Gamble Manufacturing Company
FDA Application #
part350
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-01-2015
End Marketing Date
08-12-2019
Listing Expiration
08-12-2019
Exclude Flag
D
Sample Package
No

Hierarchy Structure

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 (69423-080). Click a package code to view its specific billing and regulatory data.

14 g in 1 CYLINDER

* 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 69423-080-10 identifies a specific commercial package of 107 g in 1 cylinder of Gillette Endurance Ultimate Fresh Clear, labeled by Procter And Gamble Manufacturing Company. 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 Procter And Gamble Manufacturing Company on November 01, 2015. The current certification is valid through August 12, 2019.

How is this Procter And Gamble Manufacturing Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69423008010. 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)
69423-080-10
11-Digit CMS (5-4-2)
69423-0080-10

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