Benzalkonium Chloride Cloth
NDC Package 82355-552-01

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

Package Information

Benzalkonium Chloride (sanitizing hand wipes) cloths is take wipe and rub thoroughly over all surface of both hands. This formulation utilizes a cloth delivery system. Marketed by Alo New York Llc, this product is identified by NDC 82355-552 and is authorized under FDA application M004.

Identification & Billing

NDC Package Code
82355-552-01
Package Description
20 PACKAGE in 1 PACKAGE / 1 mg in 1 PACKAGE
Product Code
82355-552
11-Digit Billing Format
82355055201

Clinical Specifications

Proprietary Name
Benzalkonium Chloride
Non-Proprietary Name
Sanitizing Hand Wipes
Substance Name
Benzalkonium Chloride
Dosage Form
Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.
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 .0013 mg/100mg
Usage Information
Take wipe and rub thoroughly over all surface of both hands. Wet hands thoroughly with wipes. Rub hand together briskly to dry without wiping. Dispose of wipe. Do not flush.

Regulatory & Marketing

Labeler Name
Alo New York Llc
Product Type
Human Otc Drug
FDA Application #
M004
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-04-2024
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 82355-552-01 identifies a specific commercial package of 20 package in 1 package / 1 mg in 1 package of Benzalkonium Chloride, a human over the counter drug labeled by Alo New York Llc. This cloth 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 Alo New York Llc on January 04, 2024. The current certification is valid through December 31, 2027.

How is this Alo New York Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82355055201. 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)
82355-552-01
11-Digit CMS (5-4-2)
82355-0552-01

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