Naproxen Sodium Headache Pain Tablet, Film Coated
Product Images NDC 58602-735

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 Naproxen Sodium Headache Pain (NDC 58602-735). 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 (100 Tablet Bottle))

Package Label-principal Display Panel (220 mg (100 Tablet Bottle))
Label for Naproxen Sodium HEADACHE PAIN 220 mg film-coated tablets, an NSAID, by Aurohealth LLC. The label states the product contains 100 tablets and is for temporary relief of headache pain, with strength lasting 12 hours. The distributor address in East Windsor, NJ, and manufacturing in India are also shown. The label includes a depiction of a blue elliptical tablet and instructions not to use if the seal is broken or missing.*
FDA Label Image

Package Label-principal Display Panel (220 mg (100 Tablets Carton Label))

Package Label-principal Display Panel (220 mg (100 Tablets Carton Label))
Packaging label for Naproxen Sodium HEADACHE PAIN 220 mg tablets, film coated, oral use. The label shows the product name, active ingredient Naproxen Sodium USP 220 mg per tablet, and indicates 100 tablets per bottle. Distributed by Aurohealth LLC, it includes Drug Facts panels detailing usage, warnings, directions, and inactive ingredients. The label design features a blue and yellow color scheme with dosage and warning information prominently displayed.*

* 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.