Butalbital, Acetaminophen, Caffeine Tablet
Product Images NDC 69367-203

4 FDA label images from Westminster Pharmaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Butalbital, Acetaminophen, Caffeine (NDC 69367-203). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Westminster 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Butalbital 01)

Chemical Structure (Butalbital 01)
Chemical structure of the active ingredient acetaminophen, showing the molecular formula with carbon, hydrogen, nitrogen, and oxygen atoms arranged in a benzene ring with functional groups typical for acetaminophen.*
FDA Label Image

Chemical Structure (Butalbital 02)

Chemical Structure (Butalbital 02)
Chemical structure depicting a benzene ring bonded to a hydroxyl group (OH) and an acetamide group (NHCOCH3), representing the active ingredient acetaminophen.*
FDA Label Image

Chemical Structure (Butalbital 03)

Chemical Structure (Butalbital 03)
Chemical structure of caffeine, showing its molecular arrangement with ring structures and attached methyl groups.*
FDA Label Image

Principal Display Panel (100 Tablet Bottle Label)

Principal Display Panel (100 Tablet Bottle Label)
Label for Butalbital, Acetaminophen, and Caffeine Tablets, USP by Westminster Pharmaceuticals, LLC. Each oral tablet contains 50 mg Butalbital, 325 mg Acetaminophen, and 40 mg Caffeine. The bottle contains 100 tablets. The label includes dosage instructions, storage conditions, a barcode, and the Rx only designation.*

* 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.