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  5. NDC Package Code: 73062-401-01 Benzalkonium Chloride

NDC Package 73062-401-01 Benzalkonium Chloride

Dual Action Antimicrobial Wipes Cloth 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:
73062-401-01
Package Description:
150 CLOTH in 1 POUCH
Product Code:
73062-401
Proprietary Name:
Benzalkonium Chloride
Non-Proprietary Name:
Dual Action Antimicrobial Wipes
Substance Name:
Benzalkonium Chloride
Usage Information:
To use, peel back label, pull out wipe and firmly reseal label to maintain package moisture. Do not remove label.Unfold cloth and rub thoroughly over all surfaces of both hands. Use only once and throw away. After cleansing, dispose of wipe in a trash receptacle. Rub hands together briskly to dry.
11-Digit NDC Billing Format:
73062040101
NDC to RxNorm Crosswalk:
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Avro Enterprises Llc
    Dosage Form:
    Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.
    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 .13 g/1001
    • Sample Package:
    No
    FDA Application Number:
    part333A
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    10-26-2021
    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 73062-401-01?

    The NDC Packaged Code 73062-401-01 is assigned to a package of 150 cloth in 1 pouch of Benzalkonium Chloride, a human over the counter drug labeled by Avro Enterprises Llc. The product's dosage form is cloth and is administered via topical form.

    Is NDC 73062-401 included in the NDC Directory?

    Yes, Benzalkonium Chloride with product code 73062-401 is active and included in the NDC Directory. The product was first marketed by Avro Enterprises Llc on October 26, 2021 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 73062-401-01?

    The 11-digit format is 73062040101. 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
    5-3-273062-401-015-4-273062-0401-01