Mucinex Fast-max Kickstart Severe Congestion And Cough And Mucinex Fast-max Nighttime Cold And Flu Kit
Product Images NDC 72854-160

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Mucinex Fast-max Kickstart Severe Congestion And Cough And Mucinex Fast-max Nighttime Cold And Flu (NDC 72854-160). 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

Carton Label (72854 160 Label 1)

Carton Label (72854 160 Label 1)
Mucinex Fast-Max Kickstart Severe Congestion and Cough and Mucinex Fast-Max Nighttime Cold and Flu kit with menthol flavored liquid. The packaging highlights day and night relief, addressing chest congestion, cough control, mucus thinning, fever, headache, body pain, sore throat, runny nose, and sneezing. Contains two 6 fl oz (180 mL) bottles totaling 12 fl oz (360 mL). Labeler is Reckitt Benckiser LLC.*
FDA Label Image

Back Label (72854 160 Label 2)

Back Label (72854 160 Label 2)
Drug Facts panels for the Mucinex Fast-Max Kickstart Severe Congestion and Cough and Mucinex Fast-Max Nighttime Cold and Flu kit. The panels list active ingredients with strengths per 20 mL, their purposes, uses, warnings, directions, and additional product information for each component of the kit. The Nighttime Cold & Flu contains Acetaminophen 650 mg, Dextromethorphan HBr 20 mg, and Triprolidine HCl 2.5 mg; the Kickstart Severe Congestion & Cough contains Dextromethorphan HBr 20 mg and Guaifenesin 400 mg.*

* 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.