G-tuss-nl
NDC Package 43913-404-16

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.

G-tuss-nl is for the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies (allergic rhinitis).Helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.Temporarily controls cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants.Temporarily helps you cough less. Marketed by Mclaren Medical, this product is identified by NDC 43913-404 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
43913-404-16
Package Description
473 mL in 1 BOTTLE, PLASTIC
Product Code
43913-404
11-Digit Billing Format
43913040416
RxNorm Crosswalk
  • RxCUI: 1421983 - dextromethorphan HBr 10 MG / guaiFENesin 200 MG / pseudoephedrine HCl 30 MG in 5 mL Oral Solution
  • RxCUI: 1421983 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 40 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Solution
  • RxCUI: 1421983 - dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / pseudoephedrine hydrochloride 30 MG per 5 ML Oral Solution

Clinical Specifications

Proprietary Name
G-tuss-nl
Dosage Form
-
Usage Information
For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies (allergic rhinitis).Helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.Temporarily controls cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants.Temporarily helps you cough less.

Regulatory & Marketing

Labeler Name
Mclaren Medical
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
02-11-2014
Listing Expiration
12-31-2017
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 43913-404-16 identifies a specific commercial package of 473 ml in 1 bottle, plastic of G-tuss-nl, labeled by Mclaren Medical. 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 Mclaren Medical on February 11, 2014. The current certification is valid through December 31, 2017.

How is this Mclaren Medical product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43913040416. 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)
43913-404-16
11-Digit CMS (5-4-2)
43913-0404-16

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