Advanced Whitening Anti Cavity Fluoride
NDC Package 52000-035-46

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.

Advanced Whitening Anti Cavity Fluoride is usesbuilds increasing protection against painful sensitivity of teeth due to cold, heat, acids, sweets or contact.aids in the prevention of dental cavities. Marketed by Universal Distribution Center Llc, this product is identified by NDC 52000-035 and is authorized under FDA application part355.

Identification & Billing

NDC Package Code
52000-035-46
Package Description
1 TUBE in 1 BOX / 181 g in 1 TUBE
Product Code
52000-035
11-Digit Billing Format
52000003546
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
Advanced Whitening Anti Cavity Fluoride
Dosage Form
-
Usage Information
Usesbuilds increasing protection against painful sensitivity of teeth due to cold, heat, acids, sweets or contact.aids in the prevention of dental cavities.

Regulatory & Marketing

Labeler Name
Universal Distribution Center Llc
FDA Application #
part355
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
06-21-2017
Listing Expiration
12-31-2019
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 52000-035-46 identifies a specific commercial package of 1 tube in 1 box / 181 g in 1 tube of Advanced Whitening Anti Cavity Fluoride, labeled by Universal Distribution Center Llc. 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 Universal Distribution Center Llc on June 21, 2017. The current certification is valid through December 31, 2019.

How is this Universal Distribution Center Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52000003546. 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)
52000-035-46
11-Digit CMS (5-4-2)
52000-0035-46

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