Alcohol Free Foaming Hand Sanitizer Soap
NDC Package 65601-700-55

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

Alcohol Free Foaming Hand Sanitizer (benzalkonium chloride) soaps is a human otc drug administered via topical route. This formulation utilizes a soap delivery system. Marketed by Betco Corporation, Ltd., this product is identified by NDC 65601-700 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
65601-700-55
Package Description
207900 mL in 1 DRUM
Product Code
65601-700
11-Digit Billing Format
65601070055
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Alcohol Free Foaming Hand Sanitizer
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
Dosage Form
Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
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 1.3 mg/mL

Regulatory & Marketing

Labeler Name
Betco Corporation, Ltd.
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-12-2012
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (65601-700). Click a package code to view its specific billing and regulatory data.

65601-700-03
750 mL in 1 BOTTLE, PUMP
65601-700-04
3780 mL in 1 BOTTLE, PLASTIC
65601-700-05
1250 mL in 1 BOTTLE, PUMP
65601-700-29
1000 mL in 1 BAG
65601-700-53
50 mL in 1 BOTTLE, PUMP
65601-700-57
550 mL in 1 BOTTLE, PUMP
65601-700-88
500 mL in 1 BOTTLE, PUMP

* 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 65601-700-55 identifies a specific commercial package of 207900 ml in 1 drum of Alcohol Free Foaming Hand Sanitizer, a human over the counter drug labeled by Betco Corporation, Ltd.. This soap 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 Betco Corporation, Ltd. on November 12, 2012. The current certification is valid through December 31, 2027.

How is this Betco Corporation, Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 65601070055. 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)
65601-700-55
11-Digit CMS (5-4-2)
65601-0700-55

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