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  5. NDC Package Code: 49738-715-59 Kmart Corporation Maximum Strength

NDC Package 49738-715-59 Kmart Corporation Maximum Strength

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:
49738-715-59
Package Description:
1 TUBE in 1 CARTON / 113 g in 1 TUBE (49738-715-52)
Product Code:
49738-715
Proprietary Name:
Kmart Corporation Maximum Strength
Usage Information:
Adults and children 12 years of age and older: Apply at least a 1-inch strip of product onto a soft bristle toothbrush. Brush teeth thoroughly for at least one minute, preferably after each meal or at least twice a day (morning and evening) or as recommended by a dentist or physican. Make sure to brush all sensitive areas of the teeth.
11-Digit NDC Billing Format:
49738071559
NDC to 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
    • Labeler Name:
    Kmart Corporation
    Sample Package:
    No
    Start Marketing Date:
    01-20-2011
    Listing Expiration Date:
    12-31-2018
    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 49738-715-59?

    The NDC Packaged Code 49738-715-59 is assigned to a package of 1 tube in 1 carton / 113 g in 1 tube (49738-715-52) of Kmart Corporation Maximum Strength, labeled by Kmart Corporation. The product's dosage form is and is administered via form.

    Is NDC 49738-715 included in the NDC Directory?

    No, Kmart Corporation Maximum Strength with product code 49738-715 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Kmart Corporation on January 20, 2011 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 49738-715-59?

    The 11-digit format is 49738071559. 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
    5-3-249738-715-595-4-249738-0715-59