Titanium Dioxide Powder
NDC Package 58013-1021-1
Package Information
Titanium Dioxide powders is a bulk ingredient utilized for pharmaceutical compounding or manufacturing. This formulation utilizes a powder delivery system. Marketed by Croda Europe, this product is identified by NDC 58013-1021.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 58013 - Croda Europe
- 58013-1021 -
- 58013-1021-1 - 20 kg in 1 DRUM
- 58013-1021 -
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 58013-1021-1 identifies a specific commercial package of 20 kg in 1 drum of Titanium Dioxide (UNFINISHED drug), a bulk ingredient labeled by Croda Europe. This powder is formulated for use and contains titanium dioxide as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Croda Europe on July 17, 2018. The current certification is valid through December 31, 2026.
How is this Croda Europe product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 58013102101. 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.