Scarscreen
NDC Package 70089-100-11

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.

Scarscreen is shake WellAdults and children 6 months of age and over                   Apply liberally and evenly to skin area 15 minutes before you are exposed to sun or water. Marketed by Natural Crest Laboratories Inc., this product is identified by NDC 70089-100 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
70089-100-11
Package Description
1 TUBE in 1 BOX / 60 mL in 1 TUBE (70089-100-10)
Product Code
11-Digit Billing Format
70089010011

Clinical Specifications

Proprietary Name
Scarscreen
Dosage Form
-
Usage Information
Shake WellAdults and children 6 months of age and over                   Apply liberally and evenly to skin area 15 minutes before you are exposed to sun or water. Reapply at least every two hours. Use a water-resistant sunscreen if swimming or sweating.”Children under 6 months of ageAsk a doctorConsult a physician for use on children under 6 months.

Regulatory & Marketing

Labeler Name
Natural Crest Laboratories 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
09-15-2015
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 70089-100-11 identifies a specific commercial package of 1 tube in 1 box / 60 ml in 1 tube (70089-100-10) of Scarscreen, labeled by Natural Crest Laboratories 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 Natural Crest Laboratories Inc. on September 15, 2015. The current certification is valid through December 31, 2017.

How is this Natural Crest Laboratories Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70089010011. 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)
70089-100-11
11-Digit CMS (5-4-2)
70089-0100-11

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