Sanifoam
NDC Package 52030-773-26

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 inactivated by the FDA.

Sanifoam is for hand-washing to decrease bacteria on the skin, only when water is not available. Marketed by Genesan Systems, this product is identified by NDC 52030-773 and is authorized under FDA application part333.

Identification & Billing

NDC Package Code
52030-773-26
Package Description
454 g in 1 CAN
Product Code
11-Digit Billing Format
52030077326
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sanifoam
Dosage Form
-
Usage Information
For hand-washing to decrease bacteria on the skin, only when water is not available

Regulatory & Marketing

Labeler Name
Genesan Systems
FDA Application #
part333
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
01-01-2010
Listing Expiration
12-31-2018
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 (52030-773). Click a package code to view its specific billing and regulatory data.

199 g in 1 CAN

* 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 52030-773-26 identifies a specific commercial package of 454 g in 1 can of Sanifoam, labeled by Genesan Systems. 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 Genesan Systems on January 01, 2010. The current certification is valid through December 31, 2018.

How is this Genesan Systems product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52030077326. 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)
52030-773-26
11-Digit CMS (5-4-2)
52030-0773-26

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