Obagi-c Rx System Sun Shield Broad Spectrum Spf 50
NDC Package 62032-121-90

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.

Obagi-c Rx System Sun Shield Broad Spectrum Spf 50 is use twice daily, morning and evening. Marketed by Omp, Inc., this product is identified by NDC 62032-121 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
62032-121-90
Package Description
85 g in 1 TUBE
Product Code
62032-121
11-Digit Billing Format
62032012190
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Obagi-c Rx System Sun Shield Broad Spectrum Spf 50 Matte Sunscreen
Dosage Form
-
Usage Information
Use twice daily, morning and evening. Massage a small amount of cleanser and lukewarm water onto skin, rubbing gently in a circular motion. Rinse completely with lukewarm water and gently pat dry. Use twice daily, in the morning and evening after cleansing. Pump a small amount (3-4 pumps) onto a cotton pad and gently wipe over entire face. Let air dry. Do not rinse. apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply at least every 2 hourschildren under 6 months: Ask a doctorSun 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 value 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-sleeved shirts, pants, hats, and sunglasses

Regulatory & Marketing

Labeler Name
Omp, Inc.
FDA Application #
part352
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-07-2012
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 62032-121-90 identifies a specific commercial package of 85 g in 1 tube of Obagi-c Rx System Sun Shield Broad Spectrum Spf 50 Matte Sunscreen, labeled by Omp, 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 Omp, Inc. on November 07, 2012. The current certification is valid through December 31, 2017.

How is this Omp, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62032012190. 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)
62032-121-90
11-Digit CMS (5-4-2)
62032-0121-90

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