Menthol Cough Drops
NDC Package 72432-200-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Menthol Cough Drops is adults and children 6 years and older: Disolve 1 drop slowly in the mouth. Marketed by La Tia Trini Sa De Cv, this product is identified by NDC 72432-200 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
72432-200-01
Package Description
36 g in 1 BLISTER PACK
Product Code
72432-200
11-Digit Billing Format
72432020001
RxNorm Crosswalk
RxCUI: 311508 - menthol 5 MG Oral Lozenge

Clinical Specifications

Proprietary Name
Menthol Cough Drops
Dosage Form
-
Usage Information
Adults and children 6 years and older: Disolve 1 drop slowly in the mouth. May be repeated every hour as needed.Children under 6 years: Use only under adult supervision.

Regulatory & Marketing

Labeler Name
La Tia Trini Sa De Cv
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-13-2021
Listing Expiration
12-31-2022
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72432-200-01 identifies a specific commercial package of 36 g in 1 blister pack of Menthol Cough Drops, labeled by La Tia Trini Sa De Cv. 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 La Tia Trini Sa De Cv on July 13, 2021. The current certification is valid through December 31, 2022.

How is this La Tia Trini Sa De Cv product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72432020001. 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:

10-Digit Format (5-3-2)
72432-200-01
11-Digit CMS (5-4-2)
72432-0200-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.