Rynex Liquid
Product Images NDC 0485-0204

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Rynex (NDC 0485-0204). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Edwards Pharmaceuticals, 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

Rynexdm16oz

Drug Facts panel for Rynex DM liquid oral suspension showing active ingredients brompheniramine maleate 1 mg, dextromethorphan HBr 5 mg, and phenylephrine HCl 2.5 mg per 5 mL. Includes uses for allergy and cold symptom relief, warnings, directions for dosage by age, inactive ingredients, storage instructions, and contact information for questions. The product is made by Edwards Pharmaceuticals.*

FDA Label Image

Rynexdm204

Rynex DM liquid label showing a 4 oz (118 mL) bottle of oral solution with active ingredients Brompheniramine Maleate 1 mg, Dextromethorphan HBr 5 mg, and Phenylephrine HCl 2.5 mg per 5 mL. The label highlights it is sugar free, alcohol free, dye free, and gluten free, with a tutti-frutti flavor. Manufactured by Edwards Pharmaceuticals, Inc, Berwyn, PA. The label also includes tamper-evidence information and a Drug Facts panel.*

FDA Label Image

Rynexdmback

Drug Facts panel for Rynex DM oral liquid showing sections on warnings about serious side effects like seizures, overdose, and allergic reactions. Directions for use indicate dosages for different age groups: adults and children 12 years and older, children 6 to 12 years, and under 6 years old. Other information includes storage instructions and inactive ingredients. A phone number for questions or comments is also provided.*

* 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.