Dextromethorphan Hydrobromide And Guaifenesin Syrup
Product Images NDC 85722-0001

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 85722-0001). 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 (118ch)

Drug facts and directions panel for Dextromethorphan Hydrobromide and Guaifenesin Children Syrup, 10 mg/100 mg per 5 mL. The panel includes purpose, warnings, administration instructions for a 4 fl oz (118 mL) bottle with measuring cup, and manufacturer details by KJD Pharma Private Limited, India. It specifies indications for cough and chest congestion relief and dosing guidelines for various ages.*

FDA Label Image

236 (236ch)

Label for Dextromethorphan Hydrobromide and Guaifenesin Children Syrup, a cough and chest congestion syrup containing 10 mg of Dextromethorphan HBr and 100 mg of Guaifenesin per 5 mL. The bottle size is 8 fl oz (236 mL), including a measuring cup. Labeler is KJD Pharma Private Limited, India. The label lists indications for cough relief, phlegm expulsion, and decongestion of the respiratory tract, along with warnings and directions for use.*

FDA Label Image

473 (473ch)

Label for Dextromethorphan Hydrobromide and Guaifenesin Syrup, an oral children's cough and chest congestion syrup. The label states strengths of 10 mg and 100 mg per 5 mL and includes administration instructions for a 16 fl oz (473 mL) bottle with a measuring cup. It lists warnings, usage directions, and inactive ingredients, with the labeler KJD Pharma Private Limited mentioned.*

* 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.