Mucinex Fast-max Day Cold And Flu And Mucinex Nightshift Night Severe Cold And Flu Kit
Product Images NDC 72854-169

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 Day Cold And Flu And Mucinex Nightshift Night Severe Cold And Flu (NDC 72854-169). 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

Combo Back Drug Facts Label (72854 169 Back Drug Facts Label)

Combo Back Drug Facts Label (72854 169 Back Drug Facts Label)
Text panels presenting Drug Facts for Mucinex Fast-Max Day Cold & Flu and Mucinex Nightshift Night Severe Cold & Flu Maximum Strength kit. Includes active ingredients, purposes, uses, warnings, directions, inactive ingredients, and additional information for both daytime and nighttime caplets. Also provides contact information and storage instructions.*
FDA Label Image

Carton Front Label (72854 169 Label Front)

Carton Front Label (72854 169 Label Front)
Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and Flu Maximum Strength kit. The package contains 24 red day-time cold & flu caplets and 16 white night-time cold & flu caplets, total 40 caplets. Active ingredients listed include acetaminophen, dextromethorphan HBr, and triprolidine HCl. Labeler is Reckitt Benckiser LLC. The design highlights fast release caplets, all-in-one symptom relief for ages 12 and older, and tamper-evident packaging.*

* 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.