Mucinex Day Time Pain, Headache And Mucus Congestion And Mucinex Night Time Headache, Cough And Fever Kit
NDC Package 72854-210-40
Package Information
Mucinex Day Time Pain, Headache And Mucus Congestion And Mucinex Night Time Headache, Cough And Fever (acetaminophen, dextromethorphan hydrobromide, guaifenesin, triprolidine hydrochloride) kits is a medication used as Active ingredients (in each caplet) Mucinex Sinus-Max Day Pressure, Pain & Cough PurposesAcetaminophen 325 mgPain relieverGuaifenesin 200 mgExpectorantActive ingredients (in each caplet) Mucinex Nightshift Night Sinus PurposesAcetaminophen 325 mgPain reliever/fever reducerDextromethorphan HBr 10 mgCough suppressantTriprolidine HCl 1.25 mgAntihistamine. This formulation utilizes a kit delivery system. Marketed by Reckitt Benckiser Llc, this product is identified by NDC 72854-210 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 2549034 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / triprolidine HCl 1.25 MG Oral Tablet
- RxCUI: 2549034 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet
- RxCUI: 2549034 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet
- RxCUI: 2717656 - {1 (acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / triprolidine hydrochloride 1.25 MG Oral Tablet) / 1 (acetaminophen 325 MG / guaifenesin 200 MG Oral Tablet) } Pack
- RxCUI: 2717656 - 1 daytime (acetaminophen 325 MG / guaiFENesin 200 MG Oral Tablet) / 1 nighttime (acetaminophen 325 MG / dextromethorphan HBr 10 MG / triprolidine HCl 1.25 MG Oral Tablet) Pack
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 72854 - Reckitt Benckiser Llc
- 72854-210 - Mucinex Day Time Pain, Headache And Mucus Congestion And Mucinex Night Time Headache, Cough And Fever
- 72854-210-40 - 4 KIT in 1 CARTON / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
- 72854-210 - Mucinex Day Time Pain, Headache And Mucus Congestion And Mucinex Night Time Headache, Cough And Fever
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (72854-210). Click a package code to view its specific billing and regulatory data.
* 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 72854-210-40 identifies a specific commercial package of 4 kit in 1 carton / 1 kit in 1 kit * 6 tablet, film coated in 1 blister pack * 4 tablet, coated in 1 blister pack of Mucinex Day Time Pain, Headache And Mucus Congestion And Mucinex Night Time Headache, Cough And Fever 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 June 01, 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: 72854021040. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.
