Butalbital, Acetaminophen, Caffeine Tablet
Product Images NDC 85534-0046

View Photos of 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 85534-0046). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hawaii Repack, 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

Chemical Structure (Butalbital 01)

Chemical Structure (Butalbital 01)
Chemical structure of Butalbital, Acetaminophen, and Caffeine active ingredients, showing the molecular arrangement of atoms and bonds in a black-and-white line diagram.*
FDA Label Image

Chemical Structure (Butalbital 02)

Chemical Structure (Butalbital 02)
Chemical structure diagram showing a benzene ring with hydroxyl and acetamide functional groups, representing the molecular structure of acetaminophen in the Butalbital, Acetaminophen, and Caffeine medication.*
FDA Label Image

Chemical Structure (Butalbital 03)

Chemical Structure (Butalbital 03)
Chemical structure of caffeine, showing the molecular arrangement with nitrogen, carbon, hydrogen, and oxygen atoms represented in a skeletal formula.*
FDA Label Image

1 (Label)

1 (Label)
Labels for Butalbital, Acetaminophen, Caffeine 50mg/325mg/40mg tablets distributed by Hawaii RePACK. Each label shows a National Drug Code (NDC), varying quantities from 10 to 500 tablets, manufacturer Westminster Pharmaceuticals, LLC, and instruction to store at controlled room temperature. The tablets are described as white to off-white, round, and debossed.*

* 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.