Myterra Hand Sanitizer Foam Na Soap
NDC Package 70780-151-13

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

Package Information

Myterra Hand Sanitizer Foam Na (benzalkonium chloride) soaps is pump a small amount of foam into palm of hand.Rub thoroughly over all surfaces of both hands.Rub hands together briskly until dry. This formulation utilizes a soap delivery system. Marketed by Portionpac Chemical Corporation, this product is identified by NDC 70780-151 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
70780-151-13
Package Description
8 BAG in 1 BOX / 1000 mL in 1 BAG
Product Code
70780-151
11-Digit Billing Format
70780015113
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Myterra Hand Sanitizer Foam Na
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
Dosage Form
Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
BENZALKONIUM CHLORIDE 1 mg/mL
Usage Information
Pump a small amount of foam into palm of hand.Rub thoroughly over all surfaces of both hands.Rub hands together briskly until dry.

Regulatory & Marketing

Labeler Name
Portionpac Chemical Corporation
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-30-2017
Listing Expiration
12-31-2026
Exclude Flag
N
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 70780-151-13 identifies a specific commercial package of 8 bag in 1 box / 1000 ml in 1 bag of Myterra Hand Sanitizer Foam Na, a human over the counter drug labeled by Portionpac Chemical Corporation. This soap is formulated for topical use and contains benzalkonium chloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Portionpac Chemical Corporation on October 30, 2017. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70780015113. 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)
70780-151-13
11-Digit CMS (5-4-2)
70780-0151-13

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