Lumior
NDC Package 60289-296-24

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 discontinued by the firm.

Lumior is a . Marketed by Ahava Dead Sea Laboratories Ltd, this product is identified by NDC 60289-296 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
60289-296-24
Package Description
1 BOTTLE, GLASS in 1 CARTON / 50 mL in 1 BOTTLE, GLASS
Product Code
60289-296
11-Digit Billing Format
60289029624

Clinical Specifications

Proprietary Name
Lumior Men Facial Moisturizer Broad Spectrum Spf 15
Dosage Form
-

Regulatory & Marketing

Labeler Name
Ahava Dead Sea Laboratories Ltd
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-01-2020
End Marketing Date
12-30-2025
Listing Expiration
12-30-2025
Exclude Flag
D
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 60289-296-24 identifies a specific commercial package of 1 bottle, glass in 1 carton / 50 ml in 1 bottle, glass of Lumior Men Facial Moisturizer Broad Spectrum Spf 15, labeled by Ahava Dead Sea Laboratories Ltd. 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 Ahava Dead Sea Laboratories Ltd on October 01, 2020. The current certification is valid through December 30, 2025.

How is this Ahava Dead Sea Laboratories Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 60289029624. 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)
60289-296-24
11-Digit CMS (5-4-2)
60289-0296-24

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