Mucinex Fast-max Liquid Gels Day Night Cold And Flu Kit
Product Images NDC 72854-168

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 Liquid Gels Day Night Cold And Flu (NDC 72854-168). 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 168 Back Label)

Back Label (72854 168 Back Label)
Drug Facts panels for Mucinex Fast-Max Cold and Flu Maximum Strength capsules displaying active ingredients acetaminophen 325 mg and dextromethorphan HBr 10 mg per capsule. Panels include usage warnings, directions for adults and children, other information, inactive ingredients, and advice on consulting a doctor. Separate sections cover daytime and nighttime cold and flu formulations with detailed precautions and instructions.*
FDA Label Image

Carton Label (72854 168 Front Label)

Carton Label (72854 168 Front Label)
Mucinex Fast-Max Cold and Flu Maximum Strength packaging label for liquid gel capsules. The product contains acetaminophen and dextromethorphan hydrobromide as active ingredients, with additional ingredients for night-time relief. The label shows two sections: Day Time Cold & Flu with 16 liquid gels and Night Time Cold & Flu with 8 liquid gels, totaling 24 liquid gels. 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.