Acetaminophen Aspirin And Caffeine Tablet, Film Coated
Product Images NDC 58602-817

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Acetaminophen Aspirin And Caffeine (NDC 58602-817). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth 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.

FDA Label Image

Package Label-principal Display Panel (250 mg/250 mg/65 mg Container Label)

Package Label-principal Display Panel (250 mg/250 mg/65 mg Container Label)
Drug Facts text panels for Acetaminophen, Aspirin (NSAID), and Caffeine Tablets USP 250 mg/250 mg/65 mg film-coated tablets by Aurohealth LLC. The panels detail active ingredients, purposes, warnings, allergy alerts, additional precautions, directions, and storage information across multiple printable and adhesive layers for an 8-tablet package.*
FDA Label Image

Package Label-principal Display Panel (250 mg/250 mg/65 mg Container Carton Label)

Package Label-principal Display Panel (250 mg/250 mg/65 mg Container Carton Label)
Carton label for ACETAMINOPHEN, ASPIRIN (NSAID), AND CAFFEINE tablets, film-coated, 250 mg acetaminophen, 250 mg aspirin, and 65 mg caffeine per tablet. Pack contains 8 tablets, labeled as a pain reliever/fever aid. The label includes Drug Facts panels with active ingredients, uses, warnings, and inactive ingredients. The labeler is Aurohealth LLC, and the package includes barcode and lot/expiration date zones.*

* 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.