Broncochem Syrup
Product Images NDC 65131-100

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 Broncochem (NDC 65131-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laboratorio Magnachem International Srl, 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

Broncochem Maximum Cough_bottle Label-01 (Broncochem Maximum Cough Bottle Label 01)

Broncochem Maximum Cough_bottle Label-01 (Broncochem Maximum Cough Bottle Label 01)
Label for Broncochem Maximum Cough syrup containing Dextromethorphan HBr and Guaifenesin. The active ingredients are 20 mg Dextromethorphan HBr and 400 mg Guaifenesin per 10 mL. The syrup is alcohol and sugar free, intended to suppress cough and loosen phlegm. The 4 fl. oz. (120 mL) bottle is labeled as FDA registered and manufactured by Laboratorio Magnachem International SRL.*
FDA Label Image

Image Descriptionbmcusabox (Broncochem Maximum Cough Production File V9 01)

Image Descriptionbmcusabox (Broncochem Maximum Cough Production File V9 01)
Packaging label for Bronchochem Maximum Cough syrup, containing Guaifenesin USP 400 mg and Dextromethorphan HBr 20 mg per 10 mL. The label is bilingual (English and Spanish) and features a raspberry image. It highlights that the product suppresses cough, loosens phlegm, and is alcohol and sugar free. The package size is 4 fl. oz. (120 mL), and it is labeled by Laboratorio Magnachem International SRL. The label includes drug facts, usage, warnings, and inactive ingredients, along with dosing instructions and a barcode.*

* 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.