Purpleu Baobab Rejuvenating Ampoule
NDC Package 90069-205-01

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.

Purpleu Baobab Rejuvenating Ampoule is a medication used as BrighteningWrinkle improvement. Marketed by Purple U Co., Ltd, this product is identified by NDC 90069-205.

Identification & Billing

NDC Package Code
90069-205-01
Package Description
28 mL in 1 AMPULE
Product Code
11-Digit Billing Format
90069020501

Clinical Specifications

Proprietary Name
Purpleu Baobab Rejuvenating Ampoule
Dosage Form
-
Usage Information
This product is used as BrighteningWrinkle improvement. This luxurious Baobab Rejuvenating Ampoule contains highly enriched Baobab fruit extract,antioxidants, patented ingredients and patented techonolgy help with skin elasticity, hydrating,nourishing, anti-inflammatory, acne care, wound healing, and reduce fine lines and wrinkles.

Regulatory & Marketing

Labeler Name
Purple U Co., Ltd
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
09-03-2020
Listing Expiration
12-31-2021
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 90069-205-01 identifies a specific commercial package of 28 ml in 1 ampule of Purpleu Baobab Rejuvenating Ampoule, labeled by Purple U Co., Ltd. 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 Purple U Co., Ltd on September 03, 2020. The current certification is valid through December 31, 2021.

How is this Purple U Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 90069020501. 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)
90069-205-01
11-Digit CMS (5-4-2)
90069-0205-01

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