Naproxen Sodium Back And Muscle Pain Tablet, Film Coated
Product Images NDC 58602-736

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 Back And Muscle Pain (NDC 58602-736). 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))
The image shows the packaging label for Naproxen Sodium BACK AND MUSCLE PAIN tablets, USP 220 mg (NSAID) by Aurohealth LLC. The label indicates the product is a film-coated tablet for oral use in a bottle containing 100 tablets. The label highlights its use for back and muscle pain and pain relief, with strength lasting 12 hours.*
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))
Naproxen Sodium BACK AND MUSCLE PAIN 220 mg film-coated tablets packaging label by Aurohealth LLC. The label shows the product name, dosage strength, and quantity of 100 tablets. It includes drug facts detailing active ingredient, uses, warnings, directions, and inactive ingredients. The label also states the product is a human OTC drug for oral use and provides storage instructions and manufacturer information.*

* 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.