Protec Teav Hand Sanitizer
NDC Package 58575-321-04

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.

Protec Teav Hand Sanitizer is a . Marketed by Inopak, Ltd., this product is identified by NDC 58575-321 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
58575-321-04
Package Description
3785 mL in 1 PACKAGE
Product Code
11-Digit Billing Format
58575032104

Clinical Specifications

Proprietary Name
Protec Teav Hand Sanitizer
Dosage Form
-

Regulatory & Marketing

Labeler Name
Inopak, Ltd.
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
09-01-2020
End Marketing Date
08-27-2021
Listing Expiration
08-27-2021
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 (58575-321). Click a package code to view its specific billing and regulatory data.

59 mL in 1 PACKAGE
236 mL in 1 PACKAGE
1000 mL in 1 PACKAGE

* 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 58575-321-04 identifies a specific commercial package of 3785 ml in 1 package of Protec Teav Hand Sanitizer, labeled by Inopak, Ltd.. 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 Inopak, Ltd. on September 01, 2020. The current certification is valid through August 27, 2021.

How is this Inopak, Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 58575032104. 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)
58575-321-04
11-Digit CMS (5-4-2)
58575-0321-04

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