Menthol Cough Drop
NDC Package 53942-080-40
Package Information
Menthol Cough Drop is a . Marketed by Demoulas, this product is identified by NDC 53942-080 and is authorized under FDA application part341.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 53942 - Demoulas
- 53942-080 - Menthol Cough Drop
- 53942-080-40 - 40 LOZENGE in 1 BAG
- 53942-080 - Menthol Cough Drop
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 53942-080-40 identifies a specific commercial package of 40 lozenge in 1 bag of Menthol Cough Drop, labeled by Demoulas. 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 Demoulas on October 26, 2015. The current certification is valid through December 21, 2017.
How is this Demoulas product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 53942008040. 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.