Naproxen Sodium Tablet, Film Coated
Product Images NDC 79903-231

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 (NDC 79903-231). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walmart Inc., 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))
Equate All Day Pain Relief Naproxen Sodium 220 mg film-coated tablets packaging label. The label indicates the product is a pain reliever/fever reducer with strength to last 12 hours, containing 50 capsules. Distributed by Walmart Inc., the label includes dosage and warning information along with a note on the product's origin, India.*
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))
Equate All Day Pain Relief Naproxen Sodium tablets USP, 220 mg (NSAID) film coated caplets, 50 count package by Walmart Inc. The front displays active ingredient strength and purpose as pain reliever/fever reducer lasting up to 12 hours, along with a depiction of the blue caplet. Side panels provide Drug Facts, usage directions, warnings, inactive ingredients, and contact information. The label emphasizes comparison to Aleve caplets active ingredient and includes storage instructions and safety alerts.*

* 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.