Prevage Anti Agining Triple Defense Shield Broad Spectrum Sunscreen Spf 50
NDC Package 67938-0990-1

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 inactivated by the FDA.

Prevage Anti Agining Triple Defense Shield Broad Spectrum Sunscreen Spf 50 is  To Use: Turn brush head to "On" and squeeze gently to dispense product. Marketed by Elizabeth Arden, Inc, this product is identified by NDC 67938-0990 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
67938-0990-1
Package Description
1 TUBE in 1 BOX / 50 mL in 1 TUBE (67938-0990-2)
Product Code
67938-0990
11-Digit Billing Format
67938099001

Clinical Specifications

Proprietary Name
Prevage Anti Agining Triple Defense Shield Broad Spectrum Sunscreen Spf 50
Dosage Form
-
Usage Information
 To Use: Turn brush head to "On" and squeeze gently to dispense product. Brush lightly across face. Turn brush head to "Off" to store. To clean, rinse brush with warm water and towel dry.Directions For Sunscreen Use:Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hoursSun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. – 2 p.m.. Wear long-sleeve shirts, pants, hats, and sunglasses

Regulatory & Marketing

Labeler Name
Elizabeth Arden, Inc
FDA Application #
part352
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
12-14-2011
Listing Expiration
12-31-2017
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 67938-0990-1 identifies a specific commercial package of 1 tube in 1 box / 50 ml in 1 tube (67938-0990-2) of Prevage Anti Agining Triple Defense Shield Broad Spectrum Sunscreen Spf 50, labeled by Elizabeth Arden, 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 Elizabeth Arden, Inc on December 14, 2011. The current certification is valid through December 31, 2017.

How is this Elizabeth Arden, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 67938099001. 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 (5-4-1)
67938-0990-1
11-Digit CMS (5-4-2)
67938-0990-01

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