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  5. NDC Package Code: 50730-1411-1 Alcohol Prep Pad With Benzocaine

NDC Package 50730-1411-1 Alcohol Prep Pad With Benzocaine

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:
50730-1411-1
Package Description:
80 PACKET in 1 CARTON / 1 SWAB in 1 PACKET
Product Code:
50730-1411
Proprietary Name:
Alcohol Prep Pad With Benzocaine
Usage Information:
Prior to Injection - Adults and children 2 years of age or older:Apply to the skin just prior to injection. Benzocaine takes a minute to act. for best results, wait briefly and then make injection.Insect bites, skin irritations, minor burns, sunburn - Adults and children 2 years of age or older:Apply to the affected site not more than 3 to 4 times daily.Children under 2 years of age: Ask a doctor.
11-Digit NDC Billing Format:
50730141101
NDC to RxNorm Crosswalk:
  • RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Medicated Pad
  • RxCUI: 809206 - benzocaine 60 MG/ML / isopropyl alcohol 0.7 ML/ML Medicated Pad
  • RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Topical Swab
    • Labeler Name:
    H And P Industries, Inc. Dba Triad Group
    Sample Package:
    No
    Start Marketing Date:
    07-01-2008
    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 50730-1411-1?

    The NDC Packaged Code 50730-1411-1 is assigned to a package of 80 packet in 1 carton / 1 swab in 1 packet of Alcohol Prep Pad With Benzocaine, labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is and is administered via form.

    Is NDC 50730-1411 included in the NDC Directory?

    No, Alcohol Prep Pad With Benzocaine with product code 50730-1411 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 July 01, 2008 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 50730-1411-1?

    The 11-digit format is 50730141101. 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
    5-4-150730-1411-15-4-250730-1411-01