Mucinex Fast-max Day Cold And Flu And Night Cold And Flu Kit
NDC Package 72854-129-24

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 Day Cold And Flu And Night Cold And Flu (acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, and phenylephrine hydrochloride) kits is do not take more than directed (see Overdose warning)do not take more than 12 liquid gels in any 24-hour periodadults and children 12 years of age and over: take 2 liquid gels every 4 hourschildren under 12 years of age: do not use. This formulation utilizes a kit delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 72854-129 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
72854-129-24
Package Description
1 KIT in 1 CARTON * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (72854-126-24) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code
72854-129
11-Digit Billing Format
72854012924
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
RxNorm Crosswalk
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1297288 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1297288 - APAP 325 MG / Dextromethorphan Hydrobromide 10 MG / doxylamine succinate 6.25 MG / Phenylephrine Hydrochloride 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1656815 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Capsule

Clinical Specifications

Proprietary Name
Mucinex Fast-max Day Cold And Flu And Night Cold And Flu Maximum Strength
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, And Phenylephrine Hydrochloride
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Do not take more than directed (see Overdose warning)do not take more than 12 liquid gels in any 24-hour periodadults and children 12 years of age and over: take 2 liquid gels every 4 hourschildren under 12 years of age: do not use

Regulatory & Marketing

Labeler Name
Reckitt Benckiser Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-26-2021
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 72854-129-24 identifies a specific commercial package of 1 kit in 1 carton * 8 capsule, liquid filled in 1 blister pack (72854-126-24) * 8 capsule, liquid filled in 1 blister pack of Mucinex Fast-max Day Cold And Flu And Night Cold And Flu Maximum Strength, 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 July 26, 2021. 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: 72854012924. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. 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)
72854-129-24
11-Digit CMS (5-4-2)
72854-0129-24

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