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  5. NDC Package Code: 50804-780-04 Goodsense Sensitive Extra Whitening

NDC Package 50804-780-04 Goodsense Sensitive Extra Whitening

View Billable Units, 11-Digit Format, RxNorm

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.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
50804-780-04
Package Description:
1 TUBE in 1 BOX / 113 g in 1 TUBE
Product Code:
50804-780
Proprietary Name:
Goodsense Sensitive Extra Whitening
Usage Information:
Directionsadults and children 12 years of age and olderappy at least 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
11-Digit NDC Billing Format:
50804078004
NDC to RxNorm Crosswalk:
  • RxCUI: 1038800 - potassium nitrate 5 % / sodium fluoride 0.243 % (fluoride ion 0.14 % - 0.15 % ) Toothpaste
  • RxCUI: 1038800 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 1038800 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 1038800 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 1038800 - potassium nitrate 5 % / sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste
    • Labeler Name:
    Geiss, Destin & Dunn, Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-29-2015
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 50804-780-04?

    The NDC Packaged Code 50804-780-04 is assigned to a package of 1 tube in 1 box / 113 g in 1 tube of Goodsense Sensitive Extra Whitening, labeled by Geiss, Destin & Dunn, Inc.. The product's dosage form is and is administered via form.

    Is NDC 50804-780 included in the NDC Directory?

    No, Goodsense Sensitive Extra Whitening with product code 50804-780 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Geiss, Destin & Dunn, Inc. on December 29, 2015 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50804-780-04?

    The 11-digit format is 50804078004. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-250804-780-045-4-250804-0780-04