Naproxen Sodium Tablet, Film Coated
Product Images NDC 58602-819

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 (NDC 58602-819). 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (220 mg (100 Tablet Bottle))

Package Label-principal Display Panel (220 mg (100 Tablet Bottle))
Packaging label for Naproxen Sodium Tablets USP 220 mg (NSAID) by Aurohealth LLC. The label shows a blue and white color scheme and indicates the product is a film-coated, oral tablet used as a pain reliever and fever reducer. The package contains 100 tablets and highlights a strength duration of up to 12 hours. The Drug Facts panel lists the active ingredient as naproxen sodium USP 220 mg per tablet and provides information on uses, warnings, and directions for adults and children.*
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 Tablets USP 220 mg, a film-coated tablet used as a pain reliever and fever reducer. The label shows a bottle containing 100 tablets by Aurohealth LLC. The label includes drug facts, usage directions, warnings, inactive ingredients, and distributor information, with a blue tablet image on the front panel and dosage 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.