Elyptol Antimicrobial Rub
NDC Package 69343-221-08

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

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

Elyptol Antimicrobial Rub is • HAND SANITISER/SKIN ANTISEPTIC: Apply Elyptol evenly and rub for 30 seconds.• SURGICAL HAND DISINFECTION: Apply Elyptol from forearms to fingertips. Marketed by Elyptol Inc., this product is identified by NDC 69343-221 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
69343-221-08
Package Description
1 BOTTLE in 1 CARTON / 236 mL in 1 BOTTLE
Product Code
69343-221
11-Digit Billing Format
69343022108
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Elyptol Antimicrobial Rub
Dosage Form
-
Usage Information
• HAND SANITISER/SKIN ANTISEPTIC: Apply Elyptol evenly and rub for 30 seconds.• SURGICAL HAND DISINFECTION: Apply Elyptol from forearms to fingertips. Rub evenly for 3 minutes, including between fingers and over nails.• PRE-OPERATIVE SKIN PREPARATION AND SKIN ANTISEPSIS: Apply Elyptol and rub evenly over desired area for 30 seconds.

Regulatory & Marketing

Labeler Name
Elyptol Inc.
FDA Application #
part333A
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
11-01-2014
Listing Expiration
12-31-2024
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (69343-221). Click a package code to view its specific billing and regulatory data.

69343-221-02
1 BOTTLE in 1 CARTON / 59 mL in 1 BOTTLE
69343-221-03
1 BOTTLE in 1 CARTON / 89 mL in 1 BOTTLE
69343-221-16
1 BOTTLE in 1 CARTON / 473 mL in 1 BOTTLE
69343-221-34
1 BOTTLE in 1 CARTON / 1005 mL in 1 BOTTLE

* 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 69343-221-08 identifies a specific commercial package of 1 bottle in 1 carton / 236 ml in 1 bottle of Elyptol Antimicrobial Rub, labeled by Elyptol Inc.. 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 Elyptol Inc. on November 01, 2014. The current certification is valid through December 31, 2024.

How is this Elyptol Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69343022108. 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)
69343-221-08
11-Digit CMS (5-4-2)
69343-0221-08

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