Ibrite Hand Sanitizer
NDC Package 10129-080-01

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 inactivated by the FDA.

Ibrite Hand Sanitizer is dispense enough gel in your palm to cover all surfaces of hands and finger. Marketed by Gingi-pak, this product is identified by NDC 10129-080 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
10129-080-01
Package Description
59 mL in 1 BOTTLE, DISPENSING
Product Code
10129-080
11-Digit Billing Format
10129008001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Ibrite Hand Sanitizer
Dosage Form
-
Usage Information
Dispense enough gel in your palm to cover all surfaces of hands and finger. Rub hands together vigorously until dry.Usage on children requires adult supervision, not recommended for infants.Work best on clean and dry hands.

Regulatory & Marketing

Labeler Name
Gingi-pak
FDA Application #
part333A
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
04-10-2020
Listing Expiration
12-31-2024
Exclude Flag
I
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 (10129-080). Click a package code to view its specific billing and regulatory data.

10129-080-02
472 mL in 1 BOTTLE, DISPENSING
10129-080-03
250 mL in 1 BOTTLE, DISPENSING

* 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 10129-080-01 identifies a specific commercial package of 59 ml in 1 bottle, dispensing of Ibrite Hand Sanitizer, labeled by Gingi-pak. 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 Gingi-pak on April 10, 2020. The current certification is valid through December 31, 2024.

How is this Gingi-pak product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10129008001. 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)
10129-080-01
11-Digit CMS (5-4-2)
10129-0080-01

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