Myterra Hand Sanitizer Foam
NDC Package 70780-152-13

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

Package Information

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

Myterra Hand Sanitizer Foam is a . Marketed by Portionpac Chemical Corporation, this product is identified by NDC 70780-152 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
70780-152-13
Package Description
8 BAG in 1 BOX / 1 L in 1 BAG
Product Code
70780-152
11-Digit Billing Format
70780015213

Clinical Specifications

Proprietary Name
Myterra Hand Sanitizer Foam
Dosage Form
-

Regulatory & Marketing

Labeler Name
Portionpac Chemical Corporation
FDA Application #
part333E
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
10-30-2017
End Marketing Date
03-20-2020
Listing Expiration
03-20-2020
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70780-152-13 identifies a specific commercial package of 8 bag in 1 box / 1 l in 1 bag of Myterra Hand Sanitizer Foam, labeled by Portionpac Chemical Corporation. 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 Portionpac Chemical Corporation on October 30, 2017. The current certification is valid through March 20, 2020.

How is this Portionpac Chemical Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70780015213. 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)
70780-152-13
11-Digit CMS (5-4-2)
70780-0152-13

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