Dextromethorphan Hydrobromide And Guaifenesin Syrup
Product Images NDC 85722-0002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dextromethorphan Hydrobromide And Guaifenesin (NDC 85722-0002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kjd Pharma Private Limited, 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 (118)

Label of Dextromethorphan Hydrobromide and Guaifenesin Adult Syrup 20 mg / 300 mg per 5 mL by KJD Pharma Private Limited. The product is a 4 fl oz (118 mL) oral syrup intended for cough and chest congestion relief. The label includes usage warnings, dosage instructions, and administration details with a tamper-evident seal warning and a dosage measuring cup reference.*

FDA Label Image

236 (236)

Label for DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN adult syrup, 20 mg/300 mg per 5 mL, oral syrup for cough and chest congestion relief. The label states it helps relieve cough, promotes phlegm expulsion, and loosens phlegm to decongest the respiratory tract. It comes in an 8 fl oz (236 mL) bottle with a measuring cup. Manufactured by KJD Pharma Private Limited, India.*

FDA Label Image

473 (473)

Label for DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN Adult Syrup, a 16 fl oz (473 mL) oral syrup for cough and chest congestion. Active ingredients per 5 mL are 20 mg Dextromethorphan HBr and 300 mg Guaifenesin. The label includes usage instructions, warnings, and manufacturer information for KJD Pharma Private Limited.*

* 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.