Acetaminophen And Codeine Phosphate Tablet
Product Images NDC 60760-938

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 Phosphate (NDC 60760-938). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

938-30 (Acetaminophen Codeine 60760 938 30)

938-30 (Acetaminophen Codeine 60760 938 30)
Label for Acetaminophen and Codeine Phosphate Tablets USP 300mg/30mg, oral tablets. The label shows a quantity of 30 tablets. It includes referencing NDC 60760-938-30 and manufacturer information from Stides Pharma Inc., East Brunswick, NJ, with packaging by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. Directions include storing at 20°-25°C and a note to use as directed with prescription-only status.*
FDA Label Image

Acetaminophen Structure (C87671eb 3ec7 4930 Be25 5686a75679de 01)

Acetaminophen Structure (C87671eb 3ec7 4930 Be25 5686a75679de 01)
Chemical structure of acetaminophen, showing its aromatic ring with hydroxyl and amide groups, corresponding to the active ingredient acetaminophen in the product Acetaminophen and Codeine Phosphate.*
FDA Label Image

Codeine Phosphate Structure (C87671eb 3ec7 4930 Be25 5686a75679de 02)

Codeine Phosphate Structure (C87671eb 3ec7 4930 Be25 5686a75679de 02)
Chemical structure of Acetaminophen and Codeine Phosphate hydrate, showing molecular components including hydroxyl (OH), methoxy (OCH3), phosphate, and amine groups.*

* 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.