Maximum Strength Mucinex Sinus-max Severe Congestion And Pain Solution
NDC Package 63824-266-66

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

Package Information

Maximum Strength Mucinex Sinus-max Severe Congestion And Pain (acetaminophen, guaifenesin, and phenylephrine hydrochloride) solution is a medication used as Active ingredients (in each 20 mL) Mucinex Sinus-Max Severe Congestion & PainPurposesAcetaminophen 650mgPain relieverGuaifenesin 400 mgExpectorantPhenylephrine HCl 10 mgNasal decongestant Active ingredients (in each 20 mL)Mucinex Nightshift SinusPurposesAcetaminophen 650mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantPhenylephrine HCl 10 mgNasal decongestantTriprolidine HCl 2.5 mgAntihistamine. This formulation utilizes a solution delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 63824-266 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
63824-266-66
Package Description
180 mL in 1 BOTTLE
Product Code
63824-266
11-Digit Billing Format
63824026666
RxNorm Crosswalk
  • RxCUI: 1116568 - acetaminophen 650 MG / guaiFENesin 400 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution
  • RxCUI: 1116568 - acetaminophen 32.5 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1116568 - acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG per 10 ML Oral Solution
  • RxCUI: 1116568 - acetaminophen 650 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1116568 - APAP 32.5 MG/ML / Guaifenesin 20 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Maximum Strength Mucinex Sinus-max Severe Congestion And Pain
Non-Proprietary Name
Acetaminophen, Guaifenesin, And Phenylephrine Hydrochloride
Substance Name
Acetaminophen; Guaifenesin; Phenylephrine 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
This product is used as Active ingredients (in each 20 mL) Mucinex Sinus-Max Severe Congestion & PainPurposesAcetaminophen 650mgPain relieverGuaifenesin 400 mgExpectorantPhenylephrine HCl 10 mgNasal decongestant Active ingredients (in each 20 mL)Mucinex Nightshift SinusPurposesAcetaminophen 650mgPain reliever/fever reducerDextromethorphan HBr 20 mgCough suppressantPhenylephrine HCl 10 mgNasal decongestantTriprolidine HCl 2.5 mgAntihistamine

Regulatory & Marketing

Labeler Name
Reckitt Benckiser Llc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-01-2018
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 63824-266-66 identifies a specific commercial package of 180 ml in 1 bottle of Maximum Strength Mucinex Sinus-max Severe Congestion And Pain, a human over the counter drug labeled by Reckitt Benckiser Llc. This solution is formulated for oral use and contains acetaminophen; guaifenesin; phenylephrine 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 Reckitt Benckiser Llc on March 01, 2018. 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: 63824026666. 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)
63824-266-66
11-Digit CMS (5-4-2)
63824-0266-66

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