E3 Foaming Hand Sanitizer Problend
NDC Package 76250-110-01
Package Information
E3 Foaming Hand Sanitizer Problend is a . Marketed by Seatex Ltd, this product is identified by NDC 76250-110 and is authorized under FDA application part333E.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 76250 - Seatex Ltd
- 76250-110 - E3 Foaming Hand Sanitizer Problend
- 76250-110-01 - 3780 mL in 1 BOTTLE, PLASTIC
- 76250-110 - E3 Foaming Hand Sanitizer Problend
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 76250-110-01 identifies a specific commercial package of 3780 ml in 1 bottle, plastic of E3 Foaming Hand Sanitizer Problend, labeled by Seatex 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 Seatex Ltd on May 08, 2013. The current certification is valid through December 30, 2021.
How is this Seatex Ltd product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 76250011001. 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.