Mucinex Nightshift Severe Cold And Flu Solution
Product Images NDC 63824-504

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mucinex Nightshift Severe Cold And Flu (NDC 63824-504). 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

Back Label (72854 154 Back Label)

Drug Facts panels for Mucinex Nighttime Severe Cold & Flu and Mucinex Cold & Flu liquids, each showing active ingredients per 20 mL, uses, warnings, instructions on when not to use, when to ask a doctor, and other safety information. The panels include overdose warnings, directions, inactive ingredients, and a customer support phone number, emphasizing not to exceed the directed dose and to use caution with other medications.*

FDA Label Image

Carton Label (72854 154 Front Label)

Label for Mucinex Fast-Max Cold and Flu and Mucinex Nighttime Cold and Flu kit by Reckitt Benckiser LLC. The packaging highlights 'Powerful Multi-Symptom Relief' for both day and night use. It contains two 6 FL OZ (180 mL) bottles totaling 12 FL OZ (360 mL). The label shows sun and moon icons representing relief for day and night respectively, and includes drug facts, directions, inactive ingredients, and contact information.*

* 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.