Maximum Allergy Relief
Product Images NDC 81238-0240

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Maximum Allergy Relief (NDC 81238-0240). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Western First Aid Safety Dba Aramark, 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

0140 2ct Pouch (0140 2ct Pouch)

Drug facts panel from Maximum Allergy Relief pain reliever/nasal decongestant tablets by Aramark. It lists active ingredients acetaminophen 500 mg and phenylephrine HCl 5 mg with their purposes, uses for temporary relief of pain and nasal congestion, warnings including liver warnings and other health cautions, dosage directions for adults and children 12 years and older, storage information, and contact details for the labeler.*

FDA Label Image

0140-1 100ct Box (0140 1 100ct Box)

Packaging label for Maximum Allergy Relief by Western First Aid Safety DBA Aramark, featuring 100 tablets per box. The label highlights Maximum Allergy Relief as a pain reliever and nasal decongestant. The design includes dosing instructions, warnings, drug facts, and manufacturer information with a barcode. The label uses a black, white, and green color scheme.*

FDA Label Image

0140-2 250ct Box (0140 2 250ct Box)

Maximum Allergy Relief packaging label by Western First Aid Safety DBA Aramark, featuring a black and white design with green accents. The label indicates the product is a pain reliever and nasal decongestant available in a box of 250 tablets. It includes Drug Facts, usage warnings, and manufacturer contact information for Aramark in Lenexa, KS.*

* 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.