Aleve Tablet
Product Images NDC 85237-1832

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aleve (NDC 85237-1832). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Select Consumer Group, 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

Pdp (Aleve Caplets 50 Count Soft Grip Arthritis Cap Carton)

Aleve Caplets packaging label for naproxen sodium tablets, 220 mg (NSAID). Blue and red color scheme with yellow Aleve logo. The label states pain reliever/fever reducer with 50 caplets per package. Includes child-resistant cap warning, Bayer logo, and detailed drug facts, usage, warnings, directions, and inactive ingredients information. Distributed by Bayer HealthCare LLC.*

FDA Label Image

Pdp (Aleve Caplets 90 Count Easy Open Arthritis Cap Stand Alone Bottle Label 1)

Aleve Caplets packaging label for naproxen sodium tablets, 220 mg, an oral NSAID pain reliever and fever reducer. The label highlights the 'Easy Open Arthritis Cap' and states strength lasts 12 hours. It contains 90 capsule-shaped tablets and features the Bayer logo. The package is noted as not child-resistant.*

FDA Label Image

Pdp (Aleve Caplets Blusheild 200 Count Carton)

Aleve Caplets box label for naproxen sodium tablets, 220 mg (NSAID), marketed by Select Consumer Group. The blue and yellow carton states the product is an oral tablet pain reliever/fever reducer with strength lasting 12 hours. The label includes detailed Drug Facts with active ingredient, uses, warnings, directions, inactive ingredients, and contact information. The package contains 200 caplets, capsule-shaped tablets.*

* 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.