Butalbital, Acetaminophen And Caffeine Tablet
Product Images NDC 71335-2270

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 And Caffeine (NDC 71335-2270). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Fig-1 (Figure 1)

Fig-1 (Figure 1)
Chemical structure diagram showing a molecular formula with labeled chemical groups CH3, CHCH2, and (CH2)3CH3 attached to a central ring. The structure corresponds to the active ingredient as per product data but exact ingredient name is not visible in the image.*
FDA Label Image

Fig-2 (Figure 2)

Fig-2 (Figure 2)
Chemical structure diagram of the active ingredient, Acetaminophen, showing the molecular arrangement with hydroxyl and amide functional groups.*
FDA Label Image

Fig-3 (Figure 3)

Fig-3 (Figure 3)
Chemical structure diagram of the active ingredient caffeine. The diagram shows a molecular structure with a fused double-ring system and various attached functional groups.*
FDA Label Image

Label (Lbl713352270)

Label (Lbl713352270)
Label for Butalbital, Acetaminophen and Caffeine Tablets, USP with strengths of 50 mg Butalbital, 325 mg Acetaminophen, and 40 mg Caffeine. The label indicates a package count of 20 tablets, repackaged by Bryant Ranch Prepack, and manufactured by Granules Pharmaceuticals, Inc. Storage and dispensing instructions are included along with the NDC 71335-2270-1.*

* 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.