Aqua Maris Isotonised
NDC Package 76260-101-30
Package Information
Aqua Maris Isotonised is a . Marketed by Jgl North America Llc, this product is identified by NDC 76260-101.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 76260 - Jgl North America Llc
- 76260-101 - Aqua Maris Isotonised
- 76260-101-30 - 1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY
- 76260-101 - Aqua Maris Isotonised
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 76260-101-30 identifies a specific commercial package of 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray of Aqua Maris Isotonised, labeled by Jgl North America Llc. 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 Jgl North America Llc on December 28, 2001. The current certification is valid through February 22, 2023.
How is this Jgl North America Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 76260010130. 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.