Guaifenesin And Codeine Phosphate Solution
Product Images NDC 0121-1775

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 0121-1775). 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 label for Guaifenesin and Codeine Phosphate Oral Solution USP 100 mg/10 mg per 5 mL, an alcohol-free and sugar-free expectorant and cough suppressant. The label details active ingredients, uses, warnings, directions for dosing by age group, storage instructions, inactive ingredients, and important safety information including child restrictions and overdose instructions.*

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, an expectorant and cough suppressant. The label indicates a 5 mL delivery volume, is alcohol free and sugar free, and is manufactured by Pharmaceutical Associates, Inc., Greenville, SC. The package is not child-resistant and includes a barcode and NDC 0121-1775-05.*

FDA Label Image

Principal Display Panel (10 mL Unit Dose Cup Label)

Round label for Guaifenesin and Codeine Phosphate Oral Solution USP, delivering 10 mL with a strength of 200 mg guaifenesin and 20 mg codeine phosphate per 10 mL. The label indicates it is an expectorant and cough suppressant, alcohol-free, sugar-free, and not child-resistant. Manufactured by 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.