Dextromethorphan Polistirex Extended Release Suspension
Product Images NDC 72162-2281

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dextromethorphan Polistirex Extended Release (NDC 72162-2281). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Extended Label (721622281extendedlabel)

A dosing instruction chart for dextromethorphan polistirex extended release suspension. It provides specific doses by age groups, advising 10 mL every 12 hours for ages 12 and older, 5 mL every 12 hours for ages 6 to under 12, 2.5 mL every 12 hours for ages 4 to under 6, and states that children under 4 should not use the product.*

FDA Label Image

Label (Lbl721622281)

Drug Facts panel for dextromethorphan polistirex extended-release oral suspension 30 mg/5 mL, labeled by Bryant Ranch Prepack. The panel includes active ingredient information, uses as a cough suppressant, warnings, other information including storage and dosing cup provision, directions for use by age, and a list of inactive ingredients.*

* 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.