Inofoam Antibacterial Foaming Hand Wash Liquid
NDC Package 73062-032-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Inofoam Antibacterial Foaming Hand Wash (benzalkonium chloride) liquids is • Wet hands with water and dispense sufficient amount of product into cupped palm of hand. This formulation utilizes a liquid delivery system. Marketed by Avro Enterprises, Llc, this product is identified by NDC 73062-032 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
73062-032-01
Package Description
1 BOTTLE in 1 CARTON / 3800 mL in 1 BOTTLE
Product Code
73062-032
11-Digit Billing Format
73062003201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Inofoam Antibacterial Foaming Hand Wash
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
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
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
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.

Regulatory & Marketing

Labeler Name
Avro Enterprises, Llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-20-2023
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 73062-032-01 identifies a specific commercial package of 1 bottle in 1 carton / 3800 ml in 1 bottle of Inofoam Antibacterial Foaming Hand Wash, a human over the counter drug labeled by Avro Enterprises, Llc. This liquid is formulated for topical use and contains benzalkonium chloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Avro Enterprises, Llc on November 20, 2023. The current certification is valid through December 31, 2026.

How is this Avro Enterprises, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73062003201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
73062-032-01
11-Digit CMS (5-4-2)
73062-0032-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.