Up And Up Sensitive Maximum Strength Whitening
NDC Package 11673-682-04

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.

Up And Up Sensitive Maximum Strength Whitening is directionsadults and children 12 years of age and olderapply at least a 1-inch strip of product onto a soft bristle toothbrushbrush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. Marketed by Target Corporation, this product is identified by NDC 11673-682 and is authorized under FDA application part356.

Identification & Billing

NDC Package Code
11673-682-04
Package Description
1 TUBE in 1 CARTON / 113 g in 1 TUBE
Product Code
11673-682
11-Digit Billing Format
11673068204
RxNorm Crosswalk
  • RxCUI: 1038841 - potassium nitrate 5 % / sodium fluoride 0.15 % Toothpaste
  • RxCUI: 1038841 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - pot nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG gel Toothpaste
  • RxCUI: 1038841 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste

Clinical Specifications

Proprietary Name
Up And Up Sensitive Maximum Strength Whitening
Dosage Form
-
Usage Information
Directionsadults and children 12 years of age and olderapply at least a 1-inch strip of product onto a soft bristle toothbrushbrush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Minimize swallowing. Spit out after brushing.children under 12 years of age: consult a dentist or doctor

Regulatory & Marketing

Labeler Name
Target Corporation
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
12-24-2015
Listing Expiration
12-31-2018
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 11673-682-04 identifies a specific commercial package of 1 tube in 1 carton / 113 g in 1 tube of Up And Up Sensitive Maximum Strength Whitening, labeled by Target Corporation. 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 Target Corporation on December 24, 2015. The current certification is valid through December 31, 2018.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11673068204. 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)
11673-682-04
11-Digit CMS (5-4-2)
11673-0682-04

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