NDC Package 50730-1000-1 Cold Sore Treatment

View Billable Units, 11-Digit Format, RxNorm

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:
50730-1000-1
Package Description:
2 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE / .6 mL in 1 VIAL, PATENT DELIVERY SYSTEM
Product Code:
Proprietary Name:
Cold Sore Treatment
Usage Information:
Adults and children over 2 years of age:Clean the lip area of any lip preparations, lotions, ointments, residual beverages, or cosmetics including lipstick using warm water and a washclothRemove the cardboard top from applicator and place onto the glass/plastic vial end - opposite the brush end of the productSqueeze the cardboard to break the inner glass vial openSaturate the applicator end with solution by holding the brush end down and squeezing the container until you can see liquid on the brush applicatorFor best results, massage the solution into the cold sore by rubbing. Rub firmly, but take care not to damage the tissue. The purpose of the rubbing is to deliver the drug to the infection site. Hold the vial so the solution flows to the sore. To treat most cold sores, usually one treatment is enough. If your symptoms go away and then return later, apply another dose. Do not use more than 3 times per dayDiscard after use.Children under 2 years of age: ask a doctor.
11-Digit NDC Billing Format:
50730100001
NDC to RxNorm Crosswalk:
  • RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
  • RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
  • Labeler Name:
    H And P Industries, Inc. Dba Triad Group
    Sample Package:
    No
    Start Marketing Date:
    06-01-2007
    Listing Expiration Date:
    12-31-2017
    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 50730-1000-1?

    The NDC Packaged Code 50730-1000-1 is assigned to a package of 2 vial, patent delivery system in 1 package / .6 ml in 1 vial, patent delivery system of Cold Sore Treatment, labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is and is administered via form.

    Is NDC 50730-1000 included in the NDC Directory?

    No, Cold Sore Treatment with product code 50730-1000 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by H And P Industries, Inc. Dba Triad Group on June 01, 2007 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50730-1000-1?

    The 11-digit format is 50730100001. 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 5-4-1 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
    5-4-150730-1000-15-4-250730-1000-01