Acetaminophen And Codeine
Product Images NDC 66336-059

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Acetaminophen And Codeine (NDC 66336-059). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, Inc., 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

Ndc 66336-0059-xx (Ndc 66336 0059 Xx Qualitest)

Ndc 66336-0059-xx (Ndc 66336 0059 Xx     Qualitest)
Packaging label for Acetaminophen And Codeine Phosphate tablets containing 300 mg acetaminophen and 30 mg codeine phosphate. The label includes the NDC 66336-0059, states the product is for prescription use only (Rx Only), and includes warnings about habit forming potential and alcohol use. The label shows it is packaged by Dispensing Solutions, Inc., Santa Ana, CA, with additional handling instructions and sample lot information.*
FDA Label Image

This Is An Image Of The Structural Formula Of Acetaminophen. (Acetam 1)

This Is An Image Of The Structural Formula Of Acetaminophen. (Acetam 1)
Chemical structure of Acetaminophen showing the molecular arrangement including a benzene ring, hydroxyl group, and acetamide group, accompanied by molecular weight information.*
FDA Label Image

This Is An Image Of The Structural Formula Of Codeine Phosphate. (Acetam 2)

This Is An Image Of The Structural Formula Of Codeine Phosphate. (Acetam 2)
Chemical structure diagram showing the molecular structure of Acetaminophen And Codeine phosphate with associated molecular formula and molecular weight (M.W. 406.37). The diagram includes detailed atomic connections and stereochemistry.*

* 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.