Aspirin
Product Images NDC 61010-4407

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aspirin (NDC 61010-4407). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safetec Of America, 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

Principal Display Panel (325 mg Pouch Label)

Drug Facts label for Aspirin Pain Reliever/Fever Reducer by Safetec of America, Inc., Original Strength with 2 tablets per pouch. The label details active ingredient (Aspirin 325 mg), uses for temporary relief of pain types including headache and arthritis, warnings including allergy information, stomach bleeding risk, and precautions for children and certain medical conditions. Directions for use, storage instructions, and a contact number for questions are also provided.*

FDA Label Image

Principal Display Panel – 50 Count Carton Label (Asp0j 0001 02)

Safetec of America Aspirin 325 mg original strength packaging label displays the product as a pain reliever and fever reducer. The label highlights 50 tamper-evident unit dose pouches with 2 caplets per pouch. It includes usage indications, warnings, directions, inactive ingredients, and manufacturer information on a yellow and brown background with images of two white caplets.*

FDA Label Image

Principal Display Panel – 100 Count Carton Label (Asp0j 0001 03)

Packaging label for Safetec of America Aspirin 325 mg tablets, original strength, pain reliever and fever reducer. The label highlights 100 tamper-evident unit dose pouches, each containing 2 tablets. It features the Safetec logo, product name, active strength, and usage notes. The label also includes a Drug Facts panel and barcode.*

* 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.