Fluorodine Ultra Sensitive Fluoride Anticavity
NDC Package 22912-003-00

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 discontinued by the firm.

Fluorodine Ultra Sensitive Fluoride Anticavity is a . Marketed by Multibrands International Ltd, this product is identified by NDC 22912-003 and is authorized under FDA application part356.

Identification & Billing

NDC Package Code
22912-003-00
Package Description
1 TUBE in 1 PACKAGE / 132 g in 1 TUBE
Product Code
22912-003
11-Digit Billing Format
22912000300

Clinical Specifications

Proprietary Name
Fluorodine Ultra Sensitive Fluoride Anticavity
Dosage Form
-

Regulatory & Marketing

Labeler Name
Multibrands International Ltd
FDA Application #
part356
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
04-10-2013
End Marketing Date
01-07-2016
Listing Expiration
01-07-2016
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 22912-003-00 identifies a specific commercial package of 1 tube in 1 package / 132 g in 1 tube of Fluorodine Ultra Sensitive Fluoride Anticavity, labeled by Multibrands International 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 Multibrands International Ltd on April 10, 2013. The current certification is valid through January 07, 2016.

How is this Multibrands International Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 22912000300. 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)
22912-003-00
11-Digit CMS (5-4-2)
22912-0003-00

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