Hand-i-san Liquid
NDC Package 85820-900-04

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

Hand-i-san (75% isopropyl alcohol hand sanitizer) liquids is wet hands thoroughly, covering entire surface of hands, especially the fingernails and cuticlesRub hands thoroughly until dry. This formulation utilizes a liquid delivery system. Marketed by Zeco, Llc, this product is identified by NDC 85820-900 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
85820-900-04
Package Description
1040.87 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
Product Code
85820-900
11-Digit Billing Format
85820090004
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hand-i-san
Non-Proprietary Name
75% Isopropyl Alcohol Hand Sanitizer
Substance Name
Isopropyl Alcohol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
ISOPROPYL ALCOHOL .75 L/L
Usage Information
Wet hands thoroughly, covering entire surface of hands, especially the fingernails and cuticlesRub hands thoroughly until dry

Regulatory & Marketing

Labeler Name
Zeco, Llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-13-2025
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (85820-900). Click a package code to view its specific billing and regulatory data.

85820-900-02
18.29 L in 1 PAIL
85820-900-03
208.17 L in 1 DRUM
85820-900-11
4 JUG in 1 BOX / 3.78 L in 1 JUG (85820-900-01)

* 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 85820-900-04 identifies a specific commercial package of 1040.87 l in 1 container, flexible intermediate bulk of Hand-i-san, a human over the counter drug labeled by Zeco, Llc. This liquid is formulated for topical use and contains isopropyl alcohol 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 Zeco, Llc on June 13, 2025. The current certification is valid through December 31, 2026.

How is this Zeco, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85820090004. 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)
85820-900-04
11-Digit CMS (5-4-2)
85820-0900-04

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