Celonia Signature Bio Eye
NDC Package 73655-040-02

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Celonia Signature Bio Eye is directions:Pump until desired amount of the product comes and softly spread with the massage tip. Marketed by Celino Inc., this product is identified by NDC 73655-040.

Identification & Billing

NDC Package Code
73655-040-02
Package Description
1 CONTAINER in 1 CARTON / 20 mL in 1 CONTAINER (73655-040-01)
Product Code
11-Digit Billing Format
73655004002

Clinical Specifications

Proprietary Name
Celonia Signature Bio Eye
Dosage Form
-
Usage Information
Directions:Pump until desired amount of the product comes and softly spread with the massage tip. Around the eye circle until fully absorbed. Intensive Cell Training around the eye circle starts.

Regulatory & Marketing

Labeler Name
Celino Inc.
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
02-01-2020
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 73655-040-02 identifies a specific commercial package of 1 container in 1 carton / 20 ml in 1 container (73655-040-01) of Celonia Signature Bio Eye, labeled by Celino 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 Celino Inc. on February 01, 2020. The current certification is valid through December 31, 2024.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73655004002. 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)
73655-040-02
11-Digit CMS (5-4-2)
73655-0040-02

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