Zytec
NDC Package 50021-080-08

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 discontinued by the firm.

Zytec is a . Marketed by Empack Spraytech Inc., this product is identified by NDC 50021-080 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
50021-080-08
Package Description
35 g in 1 CAN
Product Code
50021-080
11-Digit Billing Format
50021008008

Clinical Specifications

Proprietary Name
Zytec Germ Buster Hand Sanitizer
Dosage Form
-

Regulatory & Marketing

Labeler Name
Empack Spraytech Inc.
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-31-2011
End Marketing Date
12-31-2022
Listing Expiration
12-31-2022
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 (50021-080). Click a package code to view its specific billing and regulatory data.

50021-080-09
400 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 50021-080-08 identifies a specific commercial package of 35 g in 1 can of Zytec Germ Buster Hand Sanitizer, labeled by Empack Spraytech 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 Empack Spraytech Inc. on January 31, 2011. The current certification is valid through December 31, 2022.

How is this Empack Spraytech Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50021008008. 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)
50021-080-08
11-Digit CMS (5-4-2)
50021-0080-08

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