Max Tussin Cough And Chest Congestion Dm Liquid
Product Images NDC 71399-0025

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Max Tussin Cough And Chest Congestion Dm (NDC 71399-0025). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akron Pharma Inc., 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

118 (118ml)

118 (118ml)
MAX Tussin Cough and Chest Congestion DM liquid, containing Dextromethorphan HBr 20 mg and Guaifenesin 200 mg per 10 mL, is shown on a pharmacy label. This cherry flavored, non-drowsy OTC cough suppressant and expectorant by Akron Pharma Inc. comes in a 4 FL OZ (118 mL) bottle for ages 12 and up.*
FDA Label Image

236 (236ml)

236 (236ml)
Drug Facts panel for MAX Tussin Cough and Chest Congestion DM liquid by Akron Pharma Inc. Lists active ingredients Dextromethorphan HBr 20 mg and Guaifenesin 200 mg per 10 mL. Includes warnings, directions for use, age restrictions, and inactive ingredients. Provides contact info and tamper-evident warning.*
FDA Label Image

473 (473ml)

473 (473ml)
Label for MAX Tussin Cough and Chest Congestion DM oral liquid, an OTC cough suppressant and expectorant containing Dextromethorphan HBr 20 mg and Guaifenesin 200 mg per 10 mL. Manufactured by Akron Pharma Inc., the 16 fl oz (473 mL) bottle is cherry flavored, alcohol-free, gluten-free, dye-free, and non-drowsy for ages 12 and up. The label includes Drug Facts and directions for use.*

* 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.