Butalbital, Acetaminophen, Caffeine, And Codeine Phosphate
Product Images NDC 0722-6670

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Butalbital, Acetaminophen, Caffeine, And Codeine Phosphate (NDC 0722-6670). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nexgen Pharma, 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

Bacc 325 (100-count Container Label)

Label for Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate capsules from Nexgen Pharma, Inc. Each capsule contains 50 mg Butalbital, 325 mg Acetaminophen, 40 mg Caffeine, and 30 mg Codeine Phosphate. The package contains 100 capsules. The label includes dosage and administration instructions, storage information, a barcode, and an NDC of 0722-6670-01.*

FDA Label Image

Butalbital Sf (Image 01)

Chemical structure diagram depicting the molecular formula C11H16N2O3 and molecular weight 224.26. This structure represents the active ingredient in the product Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate.*

FDA Label Image

Acetaminophen Sf (Image 02)

Chemical structure diagram showing a molecule with formula C8H9NO2 and molecular weight 151.16. The structure includes a benzene ring with a hydroxyl group and an amide functional group, consistent with acetaminophen.*

FDA Label Image

Caffeine Sf (Image 03)

Chemical structure diagram of the active ingredient, depicting a molecular formula of C8H10N4O2 with a molecular weight of 194.19, consistent with caffeine.*

FDA Label Image

Anhydrous Codeine Phosphate Sf (Image 04)

Chemical structure of Codeine Phosphate anhydrous with molecular formula C18H24NO7P and molecular weight 397.37.*

* 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.