Dr. Dream Urban Protective Advanced Bb
NDC Package 53077-8001-1

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.

Dr. Dream Urban Protective Advanced Bb is take out the proper amount and spread it out over the face evenly after applying your basic makeup. Marketed by Dr. Dream Inc, this product is identified by NDC 53077-8001 and is authorized under FDA application part347.

Identification & Billing

NDC Package Code
53077-8001-1
Package Description
30 mL in 1 TUBE
Product Code
53077-8001
11-Digit Billing Format
53077800101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dr. Dream Urban Protective Advanced Bb
Dosage Form
-
Usage Information
Take out the proper amount and spread it out over the face evenly after applying your basic makeup.

Regulatory & Marketing

Labeler Name
Dr. Dream Inc
FDA Application #
part347
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
09-25-2012
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 53077-8001-1 identifies a specific commercial package of 30 ml in 1 tube of Dr. Dream Urban Protective Advanced Bb, labeled by Dr. Dream 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 Dr. Dream Inc on September 25, 2012. The current certification is valid through December 31, 2017.

How is this Dr. Dream Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53077800101. 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)
53077-8001-1
11-Digit CMS (5-4-2)
53077-8001-01

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