Ambi Soothing Hand Sanitizer Gel
NDC Package 73453-143-04

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

Package Information

Ambi Soothing Hand Sanitizer (alcohol) gel is place enough product on hands to cover all surfaces. This formulation utilizes a gel delivery system. Marketed by Ambi Enterprises, Llc, this product is identified by NDC 73453-143 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
73453-143-04
Package Description
118 mL in 1 CYLINDER
Product Code
73453-143
11-Digit Billing Format
73453014304
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Ambi Soothing Hand Sanitizer
Non-Proprietary Name
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
Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Regulatory & Marketing

Labeler Name
Ambi Enterprises, Llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-20-2020
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 73453-143-04 identifies a specific commercial package of 118 ml in 1 cylinder of Ambi Soothing Hand Sanitizer, a human over the counter drug labeled by Ambi Enterprises, 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 Ambi Enterprises, Llc on May 20, 2020. The current certification is valid through December 31, 2026.

How is this Ambi Enterprises, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73453014304. 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)
73453-143-04
11-Digit CMS (5-4-2)
73453-0143-04

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