Novagel Alcohol-free Foaming Hand Sanitizer
NDC Package 78360-001-01

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.

Novagel Alcohol-free Foaming Hand Sanitizer is directions - Pump a small amount of foam onto palm of hand. Marketed by Zhejiang Hongshiliang Health Technology Co Ltd, this product is identified by NDC 78360-001 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
78360-001-01
Package Description
59.15 g in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
78360000101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Novagel Alcohol-free Foaming Hand Sanitizer
Dosage Form
-
Usage Information
Directions - Pump a small amount of foam onto palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Regulatory & Marketing

Labeler Name
Zhejiang Hongshiliang Health Technology Co Ltd
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
06-26-2020
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
No

Hierarchy Structure

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 78360-001-01 identifies a specific commercial package of 59.15 g in 1 bottle, plastic of Novagel Alcohol-free Foaming Hand Sanitizer, labeled by Zhejiang Hongshiliang Health Technology Co 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 Zhejiang Hongshiliang Health Technology Co Ltd on June 26, 2020. The current certification is valid through December 31, 2021.

How is this Zhejiang Hongshiliang Health Technology Co Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 78360000101. 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)
78360-001-01
11-Digit CMS (5-4-2)
78360-0001-01

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