Afia Alcohol-free Foaming Hand Sanitizer
NDC Package 71023-445-32

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Afia Alcohol-free Foaming Hand Sanitizer is pump a small amount of foam into palm of handRub thoroughly over all surfaces of both handsRub hands together briskly until dry. Marketed by National Chemical Laboratories, Inc., this product is identified by NDC 71023-445 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
71023-445-32
Package Description
208450 mL in 1 DRUM
Product Code
71023-445
11-Digit Billing Format
71023044532
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Afia Alcohol-free Foaming Hand Sanitizer
Dosage Form
-
Usage Information
Pump a small amount of foam into palm of handRub thoroughly over all surfaces of both handsRub hands together briskly until dry

Regulatory & Marketing

Labeler Name
National Chemical Laboratories, Inc.
FDA Application #
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
10-24-2016
Listing Expiration
12-31-2023
Exclude Flag
I
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71023-445). Click a package code to view its specific billing and regulatory data.

71023-445-29
3785 mL in 1 BOTTLE, PLASTIC
71023-445-57
1000 mL in 1 BAG

* 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 71023-445-32 identifies a specific commercial package of 208450 ml in 1 drum of Afia Alcohol-free Foaming Hand Sanitizer, labeled by National Chemical Laboratories, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by National Chemical Laboratories, Inc. on October 24, 2016. The current certification is valid through December 31, 2023.

How is this National Chemical Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71023044532. 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)
71023-445-32
11-Digit CMS (5-4-2)
71023-0445-32

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