Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Light Medium
NDC Package 63868-252-03

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.

Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Light Medium is •Apply liberally 15 minutes before sun exposure.•Reapply at least every 2 hours.•Use water resistant sunscreen if swimming or sweating.•Children under 6 months of age: ask a doctor.•Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. Marketed by Chain Drug Marketing Association, this product is identified by NDC 63868-252 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
63868-252-03
Package Description
1 TUBE in 1 CARTON / 75 mL in 1 TUBE
Product Code
11-Digit Billing Format
63868025203

Clinical Specifications

Proprietary Name
Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Light Medium
Dosage Form
-
Usage Information
•Apply liberally 15 minutes before sun exposure.•Reapply at least every 2 hours.•Use water resistant sunscreen if swimming or sweating.•Children under 6 months of age: ask a doctor.•Sun 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
Chain Drug Marketing Association
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
09-01-2014
Listing Expiration
12-31-2019
Exclude Flag
I
Sample Package
No

Hierarchy Structure

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 63868-252-03 identifies a specific commercial package of 1 tube in 1 carton / 75 ml in 1 tube of Awaken Skin Perfector Bb Broad Spectrum Spf 15 Sunscreen Light Medium, labeled by Chain Drug Marketing Association. 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 Chain Drug Marketing Association on September 01, 2014. The current certification is valid through December 31, 2019.

How is this Chain Drug Marketing Association product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63868025203. 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)
63868-252-03
11-Digit CMS (5-4-2)
63868-0252-03

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