Alcohol Free Hand Sanitizer Aerosol, Foam
NDC Package 60933-200-00

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

Package Information

Alcohol Free Hand Sanitizer (benzalkonium chloride) aerosols is - Pump a small amount of foam into palm of hand- Rub thoroughly over all surfaces of both hands- Rub hands together briskly until dry. This formulation utilizes a aerosol, foam delivery system. Marketed by Fuller Industries, Inc, this product is identified by NDC 60933-200 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
60933-200-00
Package Description
1000 mL in 1 BAG
Product Code
60933-200
11-Digit Billing Format
60933020000
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Alcohol Free Hand Sanitizer
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
Dosage Form
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
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)
BENZALKONIUM CHLORIDE 1 mg/mL
Usage Information
- Pump a small amount of foam into palm of hand- Rub thoroughly over all surfaces of both hands- Rub hands together briskly until dry

Regulatory & Marketing

Labeler Name
Fuller Industries, Inc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2017
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 60933-200-00 identifies a specific commercial package of 1000 ml in 1 bag of Alcohol Free Hand Sanitizer, a human over the counter drug labeled by Fuller Industries, Inc. This aerosol, foam is formulated for topical use and contains benzalkonium chloride 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 Fuller Industries, Inc on September 01, 2017. The current certification is valid through December 31, 2026.

How is this Fuller Industries, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 60933020000. 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)
60933-200-00
11-Digit CMS (5-4-2)
60933-0200-00

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