Zest Antibacterial Liquid Hand Soap, Fresh Aqua Gel
NDC Package 81277-013-01

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

Package Information

Zest Antibacterial Liquid Hand Soap, Fresh Aqua (benzalkonium chloride) gel is • wet hands• apply to palm of hand• scrub thoroughly• rinse thoroughly. This formulation utilizes a gel delivery system. Marketed by Sodalis Usa, Llc, this product is identified by NDC 81277-013 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
81277-013-01
Package Description
221 mL in 1 BOTTLE, PUMP
Product Code
81277-013
11-Digit Billing Format
81277001301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Zest Antibacterial Liquid Hand Soap, Fresh Aqua
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
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)
BENZALKONIUM CHLORIDE 1.3 mg/mL
Usage Information
• wet hands• apply to palm of hand• scrub thoroughly• rinse thoroughly

Regulatory & Marketing

Labeler Name
Sodalis Usa, Llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-15-2020
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 81277-013-01 identifies a specific commercial package of 221 ml in 1 bottle, pump of Zest Antibacterial Liquid Hand Soap, Fresh Aqua, a human over the counter drug labeled by Sodalis Usa, Llc. This gel 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 Sodalis Usa, Llc on July 15, 2020. The current certification is valid through December 31, 2026.

How is this Sodalis Usa, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81277001301. 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)
81277-013-01
11-Digit CMS (5-4-2)
81277-0013-01

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