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  5. NDC Package Code: 73062-033-01 Inofoam Antibacterial Foaming Hand Wash

NDC Package 73062-033-01 Inofoam Antibacterial Foaming Hand Wash

Benzalkonium Chloride Liquid 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:
73062-033-01
Package Description:
1 BAG in 1 CARTON / 1000 mL in 1 BAG
Product Code:
73062-033
Proprietary Name:
Inofoam Antibacterial Foaming Hand Wash
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
• Wet hands with water and dispense sufficient amount of product  into cupped palm of hand. • Wash both hands thoroughly for 15 seconds. •  Rinse under running water and dry thoroughly.
11-Digit NDC Billing Format:
73062003301
NDC to RxNorm Crosswalk:
  • RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Avro Enterprises, Llc
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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 1.3 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-20-2023
    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 73062-033-01?

    The NDC Packaged Code 73062-033-01 is assigned to a package of 1 bag in 1 carton / 1000 ml in 1 bag of Inofoam Antibacterial Foaming Hand Wash, a human over the counter drug labeled by Avro Enterprises, Llc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 73062-033 included in the NDC Directory?

    Yes, Inofoam Antibacterial Foaming Hand Wash with product code 73062-033 is active and included in the NDC Directory. The product was first marketed by Avro Enterprises, Llc on November 20, 2023 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 73062-033-01?

    The 11-digit format is 73062003301. 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
    5-3-273062-033-015-4-273062-0033-01