Promethazine Hydrochloride And Codeine Phosphate Solution
Product Images NDC 70752-139

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Promethazine Hydrochloride And Codeine Phosphate (NDC 70752-139). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quagen Pharmaceuticals 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

Chemicalstructure-promethazine (Chemicalstructure 02)

Chemical structure of Promethazine Hydrochloride showing its molecular configuration with labeled atoms and functional groups, including a hydrochloride (HCl) component.*

FDA Label Image

Chemicalstructure-codeine (Chemicalstructure)

Chemical structure of promethazine hydrochloride, depicted with relevant chemical groups and bonds, including phosphate (H3PO4) and water (H2O) components.*

FDA Label Image

Image Description (Containerlabel118ml)

Promethazine Hydrochloride and Codeine Phosphate Oral Solution 6.25 mg and 10 mg per 5 mL by Quagen Pharmaceuticals LLC. The 4 fl oz (118 mL) bottle contains an oral solution with 7.0% v/v alcohol. The label includes dosage warnings, storage instructions, and a barcode.*

FDA Label Image

Image Description (Containerlabel473ml)

Label for Promethazine Hydrochloride and Codeine Phosphate Oral Solution by Quagen Pharmaceuticals LLC. The solution strength is 6.25 mg Promethazine Hydrochloride and 10 mg Codeine Phosphate per 5 mL, containing 7.0% alcohol. The label includes warnings, storage instructions, and a 16 fl oz (473 mL) container size. The product is prescription only and labeled with NDC 70752-139-12.*

* 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.