Beverly Gel Hand Sanitizer Gel
NDC Package 80586-801-04

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

Package Information

Beverly Gel Hand Sanitizer (ethyl alcohol) gel is hand sanitizer to reduce microorganisms on skinUse this product when soap and water are not available. This formulation utilizes a gel delivery system. Marketed by Cleanslate Group Llc, this product is identified by NDC 80586-801 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
80586-801-04
Package Description
3785 mL in 1 BOTTLE, PLASTIC
Product Code
80586-801
11-Digit Billing Format
80586080104
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Beverly Gel Hand Sanitizer
Non-Proprietary Name
Ethyl Alcohol
Substance Name
Alcohol
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
ALCOHOL .7 mL/mL
Usage Information
Hand sanitizer to reduce microorganisms on skinUse this product when soap and water are not available

Regulatory & Marketing

Labeler Name
Cleanslate Group Llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-10-2024
Listing Expiration
12-31-2027
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 80586-801-04 identifies a specific commercial package of 3785 ml in 1 bottle, plastic of Beverly Gel Hand Sanitizer, a human over the counter drug labeled by Cleanslate Group Llc. This gel is formulated for topical use and contains alcohol 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 Cleanslate Group Llc on January 10, 2024. The current certification is valid through December 31, 2027.

How is this Cleanslate Group Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 80586080104. 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)
80586-801-04
11-Digit CMS (5-4-2)
80586-0801-04

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