Mucinex Fastmax Nighttime Dm Max Solution
Product Images NDC 72854-141

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 Fastmax Nighttime Dm Max (NDC 72854-141). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rb Health (us) 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 141 Back Label)

Back Label (72854 141 Back Label)
Mucinex Fastmax Nighttime DM MAX oral solution packaging label. The product contains 20 mg/20 mL Dextromethorphan Hydrobromide and 2.5 mg/20 mL Triprolidine Hydrochloride. The label includes drug facts, directions, warnings, active and inactive ingredients, a barcode, lot and expiration details, and contact information for RB Health (US) LLC.*
FDA Label Image

Full Carton Label (72854 141 Front Label)

Full Carton Label (72854 141 Front Label)
Label for Mucinex Fastmax Nighttime DM MAX oral solution, 6 fl oz (180 mL). Contains active ingredients Dextromethorphan HBr as cough suppressant and Triprolidine HCl as antihistamine. Marketed for nighttime relief including cough control and relief of runny nose and sneezing. Suitable for ages 12 and older. Manufactured by RB Health (US) 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.