Butalbital, Acetaminophen And Caffeine Capsule
Product Images NDC 72162-1232

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 72162-1232). 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.

FDA Label Image

52c0941-e5d7-4430-9912-909f462a63fc (552c0941 E5d7 4430 9912 909f462a63fc)

Chemical structure of butalbital, acetaminophen and caffeine. The image depicts a molecular diagram showing atoms and bonds corresponding to the chemical composition of the active ingredients in the product.*

FDA Label Image

F0f4748-ad49-4c71-8213-557eb2fe15b9 (6f0f4748 Ad49 4c71 8213 557eb2fe15b9)

Chemical structure diagram of the active ingredient acetaminophen, showing its molecular arrangement with functional groups including hydroxyl and amide.*

FDA Label Image

63f3897-3cb5-470e-b7ed-c3fda7f785c0 (D63f3897 3cb5 470e B7ed C3fda7f785c0)

Chemical structure of butalbital, one of the active ingredients in the drug product BUTALBITAL, ACETAMINOPHEN AND CAFFEINE. The diagram shows the molecular arrangement with identified bonds and rings typical of its barbiturate class.*

FDA Label Image

Label (Lbl721621232)

Label for Butalbital, Acetaminophen, and Caffeine Capsules USP 50 mg/300 mg/40 mg, containing 100 capsules. The label includes dosage information, storage instructions, and manufacturer details, with Bryant Ranch Prepack as the relabeler and Sunrise Pharmaceutical as the manufacturer. The label shows the NDC 72162-1232-1 and includes barcodes.*

* 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.