Sensai Fluid Finish Ff203
NDC Package 64159-6972-2

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.

Sensai Fluid Finish Ff203 is a . Marketed by Kanebo Cosmetics Inc, this product is identified by NDC 64159-6972 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
64159-6972-2
Package Description
10 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
64159697202

Clinical Specifications

Proprietary Name
Sensai Fluid Finish Ff203
Dosage Form
-

Regulatory & Marketing

Labeler Name
Kanebo Cosmetics Inc
FDA Application #
part352
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
08-01-2008
End Marketing Date
05-14-2015
Listing Expiration
05-14-2015
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 (64159-6972). Click a package code to view its specific billing and regulatory data.

30 mL in 1 BOTTLE, GLASS

* 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 64159-6972-2 identifies a specific commercial package of 10 ml in 1 bottle, plastic of Sensai Fluid Finish Ff203, labeled by Kanebo Cosmetics 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 Kanebo Cosmetics Inc on August 01, 2008. The current certification is valid through May 14, 2015.

How is this Kanebo Cosmetics Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 64159697202. 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 (5-4-1)
64159-6972-2
11-Digit CMS (5-4-2)
64159-6972-02

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