Xoul Intensive Cell Re-vital
NDC Package 72149-0010-1
Package Information
Xoul Intensive Cell Re-vital is a . Marketed by Picostech Co.,ltd., this product is identified by NDC 72149-0010 and is authorized under FDA application part347.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 72149 - Picostech Co.,ltd.
- 72149-0010 - Xoul Intensive Cell Re-vital
- 72149-0010-1 - 50 mL in 1 BOTTLE, PUMP
- 72149-0010 - Xoul Intensive Cell Re-vital
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 72149-0010-1 identifies a specific commercial package of 50 ml in 1 bottle, pump of Xoul Intensive Cell Re-vital, labeled by Picostech 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 Picostech Co.,ltd. on April 13, 2018. The current certification is valid through June 26, 2018.
How is this Picostech Co.,ltd. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 72149001001. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.