Mucinex Fast-max Kickstart Severe Congestion And Cough And Mucinex Fast-max Nighttime Cold And Flu Kit
NDC Package 72854-160-26

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

Package Information

Mucinex Fast-max Kickstart Severe Congestion And Cough And Mucinex Fast-max Nighttime Cold And Flu (dextromethorphan hydrobromide, guaifenesin, acetaminophen, triprolidine hydrochloride) kits is uses ■ helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive ■ 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 ■ temporarily relieves these common cold and flu symptoms: ■ cough ■ minor aches and pains ■ sore throat ■ headache ■ runny nose ■ sneezing ■ itching of the nose or throat ■ itchy, watery eyes due to hay fever ■ temporarily reduces fever ■ controls cough to help you get to sleep. This formulation utilizes a kit delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 72854-160 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
72854-160-26
Package Description
1 KIT in 1 CARTON * 180 LIQUID in 1 BOTTLE (72854-159-66) * 180 mL in 1 BOTTLE (72854-143-66)
Product Code
72854-160
11-Digit Billing Format
72854016026
RxNorm Crosswalk
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution
  • RxCUI: 1020138 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 2173667 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / triprolidine HCl 2.5 MG in 20 mL Oral Solution

Clinical Specifications

Proprietary Name
Mucinex Fast-max Kickstart Severe Congestion And Cough And Mucinex Fast-max Nighttime Cold And Flu
Non-Proprietary Name
Dextromethorphan Hydrobromide, Guaifenesin, Acetaminophen, Triprolidine Hydrochloride
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Uses ■ helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive ■ 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 ■ temporarily relieves these common cold and flu symptoms: ■ cough ■ minor aches and pains ■ sore throat ■ headache ■ runny nose ■ sneezing ■ itching of the nose or throat ■ itchy, watery eyes due to hay fever ■ temporarily reduces fever ■ controls cough to help you get to sleep

Regulatory & Marketing

Labeler Name
Reckitt Benckiser Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-02-2025
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 72854-160-26 identifies a specific commercial package of 1 kit in 1 carton * 180 liquid in 1 bottle (72854-159-66) * 180 ml in 1 bottle (72854-143-66) of Mucinex Fast-max Kickstart Severe Congestion And Cough And Mucinex Fast-max Nighttime Cold And Flu, a human over the counter drug labeled by Reckitt Benckiser Llc. This kit is formulated for use and contains 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 Reckitt Benckiser Llc on April 02, 2025. The current certification is valid through December 31, 2027.

How is this Reckitt Benckiser Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72854016026. 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)
72854-160-26
11-Digit CMS (5-4-2)
72854-0160-26

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