Amcon Labs Hand Sanitizer Instant Foam Sanitizer With Alcohol Solution
NDC Package 51801-366-18

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

Package Information

Amcon Labs Hand Sanitizer Instant Foam Sanitizer With Alcohol (alcohol) solution is pump a small amount of foam into palm of hand.Spread on hands and rub into skin until dry.Pump a smaller amount into one hand and spread over both hands and wrists.Rub into skin until dry.Children should be supervised while using this product. This formulation utilizes a solution delivery system. Marketed by Nomax, Inc., this product is identified by NDC 51801-366 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
51801-366-18
Package Description
.55 L in 1 BOTTLE, PUMP
Product Code
51801-366
11-Digit Billing Format
51801036618
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Amcon Labs Hand Sanitizer Instant Foam Sanitizer With Alcohol
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
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 620 mL/L
Usage Information
Pump a small amount of foam into palm of hand.Spread on hands and rub into skin until dry.Pump a smaller amount into one hand and spread over both hands and wrists.Rub into skin until dry.Children should be supervised while using this product.

Regulatory & Marketing

Labeler Name
Nomax, Inc.
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-04-2023
Listing Expiration
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 51801-366-18 identifies a specific commercial package of .55 l in 1 bottle, pump of Amcon Labs Hand Sanitizer Instant Foam Sanitizer With Alcohol, a human over the counter drug labeled by Nomax, Inc.. This solution 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 Nomax, Inc. on August 04, 2023. The current certification is valid through December 31, 2026.

How is this Nomax, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51801036618. 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)
51801-366-18
11-Digit CMS (5-4-2)
51801-0366-18

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