Mucinex Fastmax Nighttime Dm Max Solution
NDC Package 72854-141-66

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

Package Information

Mucinex Fastmax Nighttime Dm Max (dextromethorphan hydrobromide, triprolidine hydrochloride) solution is uses ■ temporarily relieves: ■ cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants ■ the intensity of coughing ■ the impulse to cough to help you get to sleep ■ runny nose ■ sneezing ■ itching of the nose or throat ■ itchy, watery eyes due to hay fever. This formulation utilizes a solution delivery system. Marketed by Rb Health (us) Llc, this product is identified by NDC 72854-141 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
72854-141-66
Package Description
1 BOTTLE in 1 CARTON / 180 mL in 1 BOTTLE
Product Code
72854-141
11-Digit Billing Format
72854014166

Clinical Specifications

Proprietary Name
Mucinex Fastmax Nighttime Dm Max
Non-Proprietary Name
Dextromethorphan Hydrobromide, Triprolidine Hydrochloride
Substance Name
Dextromethorphan Hydrobromide; Triprolidine Hydrochloride
Dosage Form
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Uses ■ temporarily relieves: ■ cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants ■ the intensity of coughing ■ the impulse to cough to help you get to sleep ■ runny nose ■ sneezing ■ itching of the nose or throat ■ itchy, watery eyes due to hay fever

Regulatory & Marketing

Labeler Name
Rb Health (us) Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-01-2026
Listing Expiration
12-31-2027
Exclude Flag
N
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 72854-141-66 identifies a specific commercial package of 1 bottle in 1 carton / 180 ml in 1 bottle of Mucinex Fastmax Nighttime Dm Max, a human over the counter drug labeled by Rb Health (us) Llc. This solution is formulated for oral use and contains dextromethorphan hydrobromide; triprolidine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Rb Health (us) Llc on July 01, 2026. The current certification is valid through December 31, 2027.

How is this Rb Health (us) Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72854014166. 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)
72854-141-66
11-Digit CMS (5-4-2)
72854-0141-66

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