Eo Hand Sanitizer Gel
NDC Package 54748-201-08

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

Eo Hand Sanitizer (alcohol) gel is • Wet hands thoroughly with product and allow to dry without wiping.• Do not use other than intended. This formulation utilizes a gel delivery system. Marketed by Eo Products, Llc, this product is identified by NDC 54748-201 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
54748-201-08
Package Description
236 mL in 1 BOTTLE
Product Code
54748-201
11-Digit Billing Format
54748020108
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Eo Hand Sanitizer Lavender
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
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)
ALCOHOL 62 mL/100mL
Usage Information
• Wet hands thoroughly with product and allow to dry without wiping.• Do not use other than intended.

Regulatory & Marketing

Labeler Name
Eo Products, Llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-15-2013
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 (54748-201). Click a package code to view its specific billing and regulatory data.

54748-201-02
60 mL in 1 BOTTLE
54748-201-03
240 mL in 1 BOTTLE
54748-201-04
960 mL in 1 BOTTLE
54748-201-05
59 mL in 1 BOTTLE
54748-201-07
946 mL in 1 BOTTLE
54748-201-09
6 BOTTLE in 1 BOX / 59 mL in 1 BOTTLE (54748-201-05)
54748-201-10
237 mL in 1 BOTTLE
54748-201-17
946 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 54748-201-08 identifies a specific commercial package of 236 ml in 1 bottle of Eo Hand Sanitizer Lavender, a human over the counter drug labeled by Eo Products, Llc. This gel is formulated for topical use and contains 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 Eo Products, Llc on January 15, 2013. The current certification is valid through December 31, 2026.

How is this Eo Products, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54748020108. 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)
54748-201-08
11-Digit CMS (5-4-2)
54748-0201-08

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