Emmi Dent Sodium Fluoride Anticavity Mild
NDC Package 63956-001-90

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.

Emmi Dent Sodium Fluoride Anticavity Mild is adults and children 2 years and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Marketed by Emag Ag, this product is identified by NDC 63956-001 and is authorized under FDA application part355.

Identification & Billing

NDC Package Code
63956-001-90
Package Description
1 TUBE in 1 PACKAGE / 90.6 g in 1 TUBE
Product Code
63956-001
11-Digit Billing Format
63956000190
RxNorm Crosswalk
  • RxCUI: 891775 - sodium fluoride 0.243 % Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste

Clinical Specifications

Proprietary Name
Emmi Dent Sodium Fluoride Anticavity Mild
Dosage Form
-
Usage Information
Adults and children 2 years and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Instruct children under 6 years of age in good brushing and rinsing habits  (to minimize swallowing). Supervise children as necessary until capable of using without supervision.Children under 2 years: Consult a dentist or doctor.

Regulatory & Marketing

Labeler Name
Emag Ag
FDA Application #
part355
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-22-2014
Listing Expiration
12-31-2017
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 63956-001-90 identifies a specific commercial package of 1 tube in 1 package / 90.6 g in 1 tube of Emmi Dent Sodium Fluoride Anticavity Mild, labeled by Emag Ag. 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 Emag Ag on April 22, 2014. The current certification is valid through December 31, 2017.

How is this Emag Ag product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63956000190. 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)
63956-001-90
11-Digit CMS (5-4-2)
63956-0001-90

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