Mucinex Tablet, Extended Release
Product Images NDC 72854-223

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mucinex (NDC 72854-223). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Reckitt Benckiser Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label 2 (72854 223 Back Label 2)

Drug Facts panel of Mucinex DS 12HR COLD, FEVER and SINUS (Naproxen Sodium, Pseudoephedrine Hydrochloride) extended-release tablets. Includes sections on warnings, when to stop use, pregnancy precautions, pediatric restrictions, directions, inactive ingredients, other information, and a contact number for questions. Also features a QR code for FAQs and disposal instructions.*

FDA Label Image

Back Label (72854 223 Back Label)

Drug Facts panels for Mucinex DS 12HR COLD, FEVER and SINUS extended-release tablets containing naproxen sodium 220 mg and pseudoephedrine HCl 120 mg. The panels detail active ingredients, their purposes, uses, warnings including allergy and stomach bleeding risks, heart attack and stroke warnings, and instructions on when to ask a doctor or pharmacist before use. Additional safety information and contraindications are also provided.*

FDA Label Image

Full Carton Label (72854 223 Front Label)

Mucinex DS 12HR COLD, FEVER & SINUS extended-release tablets packaging label featuring Naproxen Sodium 220 mg and Pseudoephedrine Hydrochloride 120 mg. The label highlights 12-hour multi-symptom relief for sinus pressure, headache, nasal congestion, and body aches. The package contains 20 non-drowsy tablets and displays an actual size image of the white tablet.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.