Mucinex Night Time Severe Cold And Flu Solution
Product Images NDC 72854-140

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Mucinex Night Time Severe Cold And Flu (NDC 72854-140). 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 (Night Time Label 1)

Label of Mucinex Night Time Severe Cold and Flu oral solution, 6 FL OZ (180 mL) by Reckitt Benckiser LLC. The label highlights maximum strength and lists active ingredients: acetaminophen, dextromethorphan HBr, phenylephrine HCl, and triprolidine HCl. It emphasizes multi-symptom relief including sore throat, fever, cough, nasal congestion, sneezing, and runny nose for ages 12 and older.*

FDA Label Image

Label (Night Time Label 2)

Drug Facts panel for Mucinex Night Time Severe Cold and Flu oral solution listing active ingredients per 20 mL: Acetaminophen 650 mg (pain reliever/fever reducer), Dextromethorphan HBr 20 mg (cough suppressant), Phenylephrine HCl 10 mg (nasal decongestant), and Triprolidine HCl 2.5 mg (antihistamine). It details common cold and flu symptom relief uses, warnings about liver damage from acetaminophen overdose, and usage precautions.*

FDA Label Image

Label (Night Time Label 3)

Drug Facts panel continuation for Mucinex Night Time Severe Cold and Flu oral solution. It includes allergy alerts for acetaminophen, such as severe skin reactions, a sore throat warning, specific 'Do not use' instructions particularly when taking other acetaminophen-containing drugs or monoamine oxidase inhibitors (MAOIs), and advises consulting a doctor before use if certain medical conditions are present.*

FDA Label Image

Label (Night Time Label 4)

Continuation of Drug Facts for Mucinex Night Time Severe Cold and Flu oral solution. Includes warnings to consult a doctor or pharmacist before use if taking warfarin or sedatives, directions on not exceeding dosage, cautions about drowsiness and alcohol consumption, guidance for stopping use and consulting a doctor with specific symptoms, advice for pregnant or breastfeeding individuals, and overdose warning instructions.*

FDA Label Image

Label (Night Time Label 5)

A Drug Facts panel continuation for Mucinex Night Time Severe Cold and Flu oral solution including directions, other information, inactive ingredients, and contact details. Directions emphasize dosage limits and proper use of the provided dosing cup. Other information lists sodium content and storage instructions. Inactive ingredients include ammonium glycyrrhizate, citric acid, flavorings, preservatives, and thickeners. A QR code and website URL for Reckitt Benckiser LLC are also shown.*

FDA Label Image

Label (Night Time Label 6)

This image is a partial drug facts and information panel for Mucinex Night Time Severe Cold and Flu. It includes dosing cautions about maximum strength per 4-hour dose and tamper evidency warnings. There is a notice for parents about teen medicine abuse with a website link. The panel also displays a barcode and manufacturing details including distributor and lot and expiration date placeholders.*

* 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.