Mucinex Nasal Congestion And Allergy Relief Spray, Metered
NDC Package 72854-227-60

11-digit billing NDC: 72854022760
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Mucinex Nasal Congestion And Allergy Relief (fluticasone propionate) sprays is a medication used as Fluticasone propionate (glucocorticoid)' 50 mcg . This formulation utilizes a spray, metered delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 72854-227 and is authorized under FDA application ANDA217088.

Identification & Billing

NDC Package Code
72854-227-60
Package Description
1 BOTTLE in 1 CARTON / 60 SPRAY, METERED in 1 BOTTLE
Product Code
72854-227
11-Digit Billing Format
72854022760
RxNorm Crosswalk
  • RxCUI: 1797907 - fluticasone propionate 50 MCG/ACTUAT Metered Dose Nasal Spray
  • RxCUI: 1797907 - fluticasone propionate 0.05 MG/ACTUAT Metered Dose Nasal Spray

Clinical Specifications

Proprietary Name
Mucinex Nasal Congestion And Allergy Relief
Non-Proprietary Name
Fluticasone Propionate
Substance Name
Fluticasone Propionate
Dosage Form
Spray, Metered - A non-pressurized dosage form consisting of valves which allow the dispensing of a specified quantity of spray upon each activation.
Administration Route
Nasal - Administration to the nose; administered by way of the nose.
Active Ingredient(s)
FLUTICASONE PROPIONATE 50 ug/1
Pharmacologic Class
Usage Information
This product is used as Fluticasone propionate (glucocorticoid)' 50 mcg ..... ................. ................. .. ....... Allergy symptom reliever. UsesTemporarily relieves these symptoms of hay fever or other upper respiratory allergies: ■ nasal congestion ■ itchy nose ■ runny nose ■ itchy, watery eyes ■ sneezing

Regulatory & Marketing

Labeler Name
Reckitt Benckiser Llc
Product Type
Human Otc Drug
FDA Application #
ANDA217088
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
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 72854-227-60 identifies a specific commercial package of 1 bottle in 1 carton / 60 spray, metered in 1 bottle of Mucinex Nasal Congestion And Allergy Relief, a human over the counter drug labeled by Reckitt Benckiser Llc. This spray, metered is formulated for nasal use and contains fluticasone propionate 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 01, 2026. 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: 72854022760. 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)
72854-227-60
11-Digit CMS (5-4-2)
72854-0227-60

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