Acetaminophen And Codeine Phosphate Tablet
Product Images NDC 68071-4673

3 FDA label images from Nucare Pharmaceuticals,inc. · 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 Phosphate (NDC 68071-4673). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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

68071 4673 5

68071 4673 5
Label for Acetaminophen and Codeine Phosphate 300 mg / 30 mg tablets manufactured by NuCare Pharmaceuticals, Inc. The label shows NDC 68071-4673-5, indicates a bottle containing 15 tablets, and states the tablet is round, white or off-white, debossed with "U36". It includes warnings, dosing instructions to take 1 tablet 4 times a day, and storage conditions between 68-77°F. The label notes the product is RX only and advises keeping it out of reach of children.*
FDA Label Image

Chemical Structure (Acetaminophen Str1)

Chemical Structure (Acetaminophen Str1)
Chemical structure of Acetaminophen and Codeine Phosphate showing a phenol group, amide linkage, and methyl group. The molecular formula (C8H9NO2) and molecular weight (151.16) are displayed below the structure.*
FDA Label Image

Chemical Structure (Acetaminophen Str2)

Chemical Structure (Acetaminophen Str2)
Chemical structure of Acetaminophen and Codeine Phosphate with molecular formula C18H21NO3·H3PO4·½H2O and molecular weight 406.37. The diagram depicts the detailed molecular arrangement including functional groups and phosphate hydration.*

* 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.