Antibacterial Hand Sanitizer
NDC Package 73563-080-01

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.

Antibacterial Hand Sanitizer is wet hands thoroughly with productbriskly rub hands together until drysupervise children in the use of this product. Marketed by Body One Products , Inc., this product is identified by NDC 73563-080 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
73563-080-01
Package Description
29.5 mL in 1 TUBE
Product Code
73563-080
11-Digit Billing Format
73563008001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Antibacterial Hand Sanitizer
Dosage Form
-
Usage Information
Wet hands thoroughly with productbriskly rub hands together until drysupervise children in the use of this product

Regulatory & Marketing

Labeler Name
Body One Products , 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
03-10-2020
Listing Expiration
12-31-2022
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 (73563-080). Click a package code to view its specific billing and regulatory data.

73563-080-02
59 mL in 1 BOTTLE
73563-080-04
3785 mL in 1 BOTTLE
73563-080-06
66 mL in 1 TUBE
73563-080-07
7 mL in 1 PACKET
73563-080-08
236 mL in 1 BOTTLE
73563-080-12
355 mL in 1 BOTTLE, PUMP
73563-080-18
532 mL in 1 BOTTLE
73563-080-32
1064 mL in 1 BOTTLE

* 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 73563-080-01 identifies a specific commercial package of 29.5 ml in 1 tube of Antibacterial Hand Sanitizer, labeled by Body One Products , 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 Body One Products , Inc. on March 10, 2020. The current certification is valid through December 31, 2022.

How is this Body One Products , Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73563008001. 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)
73563-080-01
11-Digit CMS (5-4-2)
73563-0080-01

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