Upside Down Collector Fanny Pack Kit
NDC Package 72866-034-01

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

Package Information

Upside Down Collector Fanny Pack (alcohol) kits is wet hands thoroughly with product and allow to dry without wiping. This formulation utilizes a kit delivery system. Marketed by Merci Handy Corporation, this product is identified by NDC 72866-034 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
72866-034-01
Package Description
1 KIT in 1 POUCH * 30 mL in 1 BOTTLE (72866-035-01)
Product Code
72866-034
11-Digit Billing Format
72866003401
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Upside Down Collector Fanny Pack
Non-Proprietary Name
Alcohol
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Wet hands thoroughly with product and allow to dry without wiping

Regulatory & Marketing

Labeler Name
Merci Handy Corporation
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-20-2021
End Marketing Date
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 72866-034-01 identifies a specific commercial package of 1 kit in 1 pouch * 30 ml in 1 bottle (72866-035-01) of Upside Down Collector Fanny Pack, a human over the counter drug labeled by Merci Handy Corporation. This kit is formulated for use and contains 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 Merci Handy Corporation on September 20, 2021.

How is this Merci Handy Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72866003401. 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)
72866-034-01
11-Digit CMS (5-4-2)
72866-0034-01

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