Ultra Tuss Dm
NDC Package 42213-161-93
Package Information
Ultra Tuss Dm is a . Marketed by Ultra Seal Corporation, this product is identified by NDC 42213-161 and is authorized under FDA application M012.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 42213 - Ultra Seal Corporation
- 42213-161 - Ultra Tuss Dm
- 42213-161-93 - 474 mL in 1 BOTTLE
- 42213-161 - Ultra Tuss Dm
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 42213-161-93 identifies a specific commercial package of 474 ml in 1 bottle of Ultra Tuss Dm, labeled by Ultra Seal Corporation. 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 Ultra Seal Corporation on June 19, 2012. The current certification is valid through December 01, 2021.
How is this Ultra Seal Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 42213016193. 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 Product segment to maintain the 5-4-2 structure.