Foaming Alcohol Hand Rub
NDC Package 65353-3413-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Foaming Alcohol Hand Rub is a . Marketed by Brenntag Mid-south, Inc., this product is identified by NDC 65353-3413 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
65353-3413-2
Package Description
1040 L in 1 TANK
Product Code
11-Digit Billing Format
65353341302

Clinical Specifications

Proprietary Name
Foaming Alcohol Hand Rub
Dosage Form
-

Regulatory & Marketing

Labeler Name
Brenntag Mid-south, 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
10-19-2020
End Marketing Date
10-19-2020
Listing Expiration
10-19-2020
Exclude Flag
D
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 (65353-3413). Click a package code to view its specific billing and regulatory data.

18.9 L in 1 PAIL

* 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 65353-3413-2 identifies a specific commercial package of 1040 l in 1 tank of Foaming Alcohol Hand Rub, labeled by Brenntag Mid-south, 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 Brenntag Mid-south, Inc. on October 19, 2020. The current certification is valid through October 19, 2020.

How is this Brenntag Mid-south, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 65353341302. 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 (5-4-1)
65353-3413-2
11-Digit CMS (5-4-2)
65353-3413-02

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