Fresh Wave Iaq Antiseptic Hand Rub
NDC Package 75399-014-00
Package Information
Fresh Wave Iaq Antiseptic Hand Rub is a . Marketed by Omi Industries, this product is identified by NDC 75399-014 and is authorized under FDA application part333A.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 75399 - Omi Industries
- 75399-014 - Fresh Wave Iaq Antiseptic Hand Rub
- 75399-014-00 - 236 mL in 1 BOTTLE, SPRAY
- 75399-014 - Fresh Wave Iaq Antiseptic Hand Rub
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 75399-014-00 identifies a specific commercial package of 236 ml in 1 bottle, spray of Fresh Wave Iaq Antiseptic Hand Rub, labeled by Omi Industries. 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 Omi Industries on April 15, 2020. The current certification is valid through July 23, 2021.
How is this Omi Industries product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 75399001400. 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.