Dextromethorphan Polistirex Suspension, Extended Release
Product Images NDC 58602-617

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 Dextromethorphan Polistirex (NDC 58602-617). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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

Principal Display Panel (89 mL (3 fl oz) Bottle Label)

Principal Display Panel (89 mL (3 fl oz) Bottle Label)
Label for Dextromethorphan Polistirex Extended-Release Oral Suspension 30 mg/5 mL, an orange-flavored cough suppressant. The label includes drug facts, usage instructions, warnings, and storage information. Distributed by Aurohealth LLC. The 89 mL bottle label highlights 12-hour relief, alcohol-free formulation, and no fever reducer or pain reliever included.*
FDA Label Image

Principal Display Panel (89 mL (3 fl oz) Bottle Carton Label)

Principal Display Panel (89 mL (3 fl oz) Bottle Carton Label)
The packaging label for Dextromethorphan Polistirex Extended-Release Oral Suspension 30 mg/5 mL by Aurohealth LLC features an orange-flavored liquid in an 89 mL (3 fl oz) bottle. It highlights 12-hour relief for cough suppression, includes dosing instructions with a dosing cup, and specifies the product is day or night use and alcohol-free. The label also notes that the product contains no fever reducer or pain reliever.*

* 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.