Zest Antibacterial Liquid Hand Soap, Fresh Aqua
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

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Zest Antibacterial Liquid Hand Soap, Fresh Aqua is • wet hands• apply to palm of hand• scrub thoroughly• rinse thoroughly. 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
Dosage Form
-
Usage Information
• wet hands• apply to palm of hand• scrub thoroughly• rinse thoroughly

Regulatory & Marketing

Labeler Name
Sodalis Usa, Llc
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-15-2020
Listing Expiration
12-31-2026
Exclude Flag
I
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, labeled by Sodalis Usa, Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary 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.