Guaifenesin And Codeine Phosphate Solution
Product Images NDC 0121-1550

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Guaifenesin And Codeine Phosphate (NDC 0121-1550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, 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

Principal Display Panel (473 mL Bottle Label)

Drug Facts panel for Guaifenesin and Codeine Phosphate Oral Solution USP 100 mg/10 mg per 5 mL, an expectorant and cough suppressant that is alcohol and sugar free. The label includes active ingredients and purposes, uses, warnings, directions by age group, storage instructions, inactive ingredients, and contact information for questions or comments. It advises keeping the product out of children’s reach and notes safety precautions for use in certain populations.*

FDA Label Image

Principal Display Panel (10 mL Unit Dose Cup Label)

Label for Guaifenesin and Codeine Phosphate Oral Solution USP 100 mg/10 mg per 5 mL. The label indicates it is an expectorant and cough suppressant, alcohol-free and sugar-free. It delivers 5 mL per dose and includes a barcode. Manufactured by Pharmaceutical Associates, Inc., Greenville, SC.*

FDA Label Image

Principal Display Panel (10 mL Unit Dose Cup Label)

Round bottle label for Guaifenesin and Codeine Phosphate Oral Solution USP, delivering 10 mL with a strength of 200 mg/20 mg per 10 mL. The label states it is an expectorant and cough suppressant, alcohol-free and sugar-free. The label includes a barcode and the manufacturer, Pharmaceutical Associates, Inc., Greenville, SC.*

* 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.