Dextromethorphan Polistirex Extended-release Suspension
Product Images NDC 65162-700

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 Extended-release (NDC 65162-700). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

30 mg/5 mL 3oz Label (Dextromethorphan Polistirex Suspension Orange 1)

30 mg/5 mL 3oz Label (Dextromethorphan Polistirex Suspension Orange 1)
This is a description of a prescription medication called "Dextromethorphan Polistirex." This medication is an oral suspension that contains a cough suppressant and is used to relieve pain and coughing. The medication is alcohol-free and comes in a 89mL (3fl0z) bottle. The medication has an extended-release, and each 5 mL of the suspension contains 30 mg of the active ingredient. The package has a NDC number of 65162-700-76, and the brand name of the medication is "Compere fo Detoym."*
FDA Label Image

30 mg/5 mL 3oz Carton (Dextromethorphan Polistirex Suspension Orange 2)

30 mg/5 mL 3oz Carton (Dextromethorphan Polistirex Suspension Orange 2)
This text appears to be a drug label with medication information. It includes drug facts, drug purpose, dosage information with a dosing chart, and warnings. The medication is an extended-release oral suspension solution for cough relief with the active ingredient being Dextromethorphan Polistirex. The text includes a phone number for questions and contact information for the manufacturer.*

* 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.