Sensitive Extra Whitening Paste, Dentifrice
NDC Package 56062-413-33

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Sensitive Extra Whitening (sodium fluoride) pastes is builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact * acids in the prevention of dental cavities. This formulation utilizes a paste, dentifrice delivery system. Marketed by Publix Super Market, this product is identified by NDC 56062-413 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
56062-413-33
Package Description
1 TUBE in 1 CARTON / 113 g in 1 TUBE
Product Code
56062-413
11-Digit Billing Format
56062041333
RxNorm Crosswalk
  • RxCUI: 1038929 - potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste
  • RxCUI: 1038929 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.0024 MG/MG Toothpaste
  • RxCUI: 1038929 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste
  • RxCUI: 1038929 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste
  • RxCUI: 1038929 - potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste

Clinical Specifications

Proprietary Name
Sensitive Extra Whitening
Non-Proprietary Name
Sodium Fluoride
Substance Name
Potassium Nitrate; Sodium Fluoride
Dosage Form
Paste, Dentifrice - A paste formulation intended to clean and/or polish the teeth, and which may contain certain additional agents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact * acids in the prevention of dental cavities

Regulatory & Marketing

Labeler Name
Publix Super Market
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-18-2024
Listing Expiration
12-31-2026
Exclude Flag
N
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 56062-413-33 identifies a specific commercial package of 1 tube in 1 carton / 113 g in 1 tube of Sensitive Extra Whitening, a human over the counter drug labeled by Publix Super Market. This paste, dentifrice is formulated for oral use and contains potassium nitrate; sodium fluoride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Publix Super Market on July 18, 2024. The current certification is valid through December 31, 2026.

How is this Publix Super Market product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 56062041333. 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)
56062-413-33
11-Digit CMS (5-4-2)
56062-0413-33

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