Naproxen Sodium Headache Pain Tablet, Film Coated
Product Images NDC 58602-737

2 FDA label images from Aurohealth Llc · 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 Naproxen Sodium Headache Pain (NDC 58602-737). 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 (220 mg (24 Tablets, Container Label))

Package Label-principal Display Panel (220 mg (24 Tablets, Container Label))
The image shows the label for Naproxen Sodium HEADACHE PAIN tablets, USP 220 mg (NSAID), film-coated, in a 24-tablet package distributed by Aurohealth LLC. The blue label highlights pain relief, fever reduction, headache pain relief, and up to 12-hour strength. It includes lot and expiration date sections and safety warnings about the bottle seal.*
FDA Label Image

Package Label-principal Display Panel (220 mg (24 Tablets Carton Label))

Package Label-principal Display Panel (220 mg (24 Tablets Carton Label))
Packaging label for Naproxen Sodium HEADACHE PAIN tablets, 220 mg strength, film-coated tablets. The label shows the product is distributed by Aurohealth LLC and contains 24 tablets per bottle. It includes Drug Facts panels with information on active ingredients, uses, warnings, and directions for use. The label also provides storage instructions and a 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.