Mucinex Fast-max Severe Congestion And Cough And Mucinex Nighttime Cold And Flu Kit
Product Images NDC 72854-166

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mucinex Fast-max Severe Congestion And Cough And Mucinex Nighttime Cold And Flu (NDC 72854-166). 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 166 Back Label)

Back Label (72854 166 Back Label)
Drug Facts panels for Mucinex Nighttime Cold and Flu and Mucinex Fast-Max Severe Congestion and Cough. Panels list active ingredients per 20 mL, purposes, uses, warnings, directions, other information including sodium content, inactive ingredients, and a customer service phone number. Each panel provides detailed warnings, usage instructions, and precautions specific to each formulation.*
FDA Label Image

Carton Label (72854 166 Front Label)

Carton Label (72854 166 Front Label)
Mucinex Fast-Max Severe Congestion and Cough and Mucinex Nighttime Cold and Flu kit packaging label. The kit contains two 6 FL OZ (180 mL) bottles, totaling 12 FL OZ (360 mL). The front highlights multi-symptom relief for day and night, including cough control, nasal and chest congestion relief, thinning and loosening mucus, and nighttime relief for fever, headache, body pain, cough, sore throat, runny nose, and sneezing. The labeler is Reckitt Benckiser LLC.*

* 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.