Aramark Multi-symptom Cold Relief
Product Images NDC 81238-0107

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aramark Multi-symptom Cold Relief (NDC 81238-0107). 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

0107 2-tab Packet (0107 2 Tab Packet)

Drug Facts panel for Aramark Multi-Symptom Cold Relief, containing active ingredients acetaminophen 325 mg, guaifenesin 200 mg, and phenylephrine HCl 5 mg. The panel details its use for relieving nasal congestion and related symptoms, warnings including liver warning and other health cautions, directions for use by adults and children, storage information, tamper evidence, and manufacturer contact details.*

FDA Label Image

0107-100ct Tab Box (0107 100ct Tab Box)

Packaging label for Aramark Multi-Symptom Cold Relief, a non-pseudo tablet decongestant. The label displays 100 tablets per box and includes detailed Drug Facts panels with active ingredients, uses, warnings, and directions. Manufactured by Aramark in Lenexa, KS, the label features the Aramark logo and branding.*

FDA Label Image

0107-2 250ct Tab Box (0107 2 250ct Tab Box)

Box packaging label for Aramark Multi-Symptom Cold Relief Non-Pseudo Tablet Decongestant. The label indicates the package contains 250 tablets and features the Aramark logo. It includes Drug Facts, usage instructions, warnings, and manufacturing information for Western First Aid Safety DBA Aramark, Lenexa, KS. The label design is predominantly black, gray, and green with red accent text.*

* 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.