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  5. NDC Package Code: 50552-002-01 Anti-bacterial Wipes

NDC Package 50552-002-01 Anti-bacterial Wipes

Benzalkonium Chloride Solution Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
50552-002-01
Package Description:
80 APPLICATOR in 1 CANISTER / .5 g in 1 APPLICATOR
Product Code:
50552-002
Proprietary Name:
Anti-bacterial Wipes
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
UsesAntiseptic that kills germs and helps prevent the spread of cold
11-Digit NDC Billing Format:
50552000201
NDC to RxNorm Crosswalk:
  • RxCUI: 1043322 - benzalkonium Cl 0.155 % Medicated Pad
  • RxCUI: 1043322 - benzalkonium chloride 1.55 MG/ML Medicated Pad
  • RxCUI: 1043322 - benzalkonium chloride 0.155 % Medicated Wipe
  • RxCUI: 1043322 - benzalkonium chloride 0.155 % Topical Swab
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Tongling Jieya Biological Technology Co., Ltd.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • BENZALKONIUM CHLORIDE .155 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M005
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-03-2010
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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 50552-002-01?

    The NDC Packaged Code 50552-002-01 is assigned to a package of 80 applicator in 1 canister / .5 g in 1 applicator of Anti-bacterial Wipes, a human over the counter drug labeled by Tongling Jieya Biological Technology Co., Ltd.. The product's dosage form is solution and is administered via topical form.

    Is NDC 50552-002 included in the NDC Directory?

    Yes, Anti-bacterial Wipes with product code 50552-002 is active and included in the NDC Directory. The product was first marketed by Tongling Jieya Biological Technology Co., Ltd. on February 03, 2010 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50552-002-01?

    The 11-digit format is 50552000201. 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
    5-3-250552-002-015-4-250552-0002-01