Mucinex Nightshift Solution
Product Images NDC 63824-503

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 Nightshift (NDC 63824-503). 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 165 Label Back)

Back Label (72854 165 Label Back)
Drug Facts panels for Mucinex Nighttime Cold and Flu and Mucinex Fast-Max DM Max kit. Each panel lists active ingredients with amounts and purposes, uses, warnings, directions for use, other information, inactive ingredients, and a contact number for questions. The Nighttime Cold and Flu includes acetaminophen, dextromethorphan HBr, and triprolidine HCl; the DM Max includes dextromethorphan HBr and guaifenesin.*
FDA Label Image

Carton Label (72854 165 Label Front)

Carton Label (72854 165 Label Front)
Mucinex Fast-Max DM Max and Mucinex Nighttime Cold and Flu kit packaging label showing two 6 fl oz (180 mL) bottles, total 12 fl oz (360 mL). The day formula bottle features a sun icon and claims to control cough, thin and loosen mucus, and relieve chest congestion. The nighttime formula bottle features a moon and stars icon and is indicated for nighttime relief of fever, headache, body pain, cough, sore throat, runny nose, and sneezing. Label includes dosing instructions, inactive ingredients, and contact information for 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.