Pioneer Eclipse Touche Foaming Non-alcohol Hand Sanitizer
NDC Package 70415-305-01

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.

Pioneer Eclipse Touche Foaming Non-alcohol Hand Sanitizer is apply foam sanitizer to hands.Rub over surfaces of both hands for 15 seconds.No rinsing required. Marketed by Cwgc La Inc., this product is identified by NDC 70415-305 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
70415-305-01
Package Description
1000 mL in 1 BOTTLE
Product Code
11-Digit Billing Format
70415030501
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Pioneer Eclipse Touche Foaming Non-alcohol Hand Sanitizer
Dosage Form
-
Usage Information
Apply foam sanitizer to hands.Rub over surfaces of both hands for 15 seconds.No rinsing required.

Regulatory & Marketing

Labeler Name
Cwgc La Inc.
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
08-04-2017
Listing Expiration
12-31-2024
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 70415-305-01 identifies a specific commercial package of 1000 ml in 1 bottle of Pioneer Eclipse Touche Foaming Non-alcohol Hand Sanitizer, labeled by Cwgc La 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 Cwgc La Inc. on August 04, 2017. The current certification is valid through December 31, 2024.

How is this Cwgc La Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70415030501. 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)
70415-305-01
11-Digit CMS (5-4-2)
70415-0305-01

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