Aleve Tablet, Coated
Product Images NDC 0280-6020

3 FDA label images from Bayer Healthcare Llc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aleve (NDC 0280-6020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bayer Healthcare 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

Aleve Gelcap 160 Back

Aleve Gelcap 160 Back
Drug Facts panels from Aleve Gelcaps (Naproxen Sodium) 220 mg coated oral tablets by Bayer HealthCare LLC. The text contains typical OTC drug information including active ingredients, uses, warnings, directions, and other consumer safety information. Additional labeling elements include distribution and trademark details.*
FDA Label Image

Aleve Gelcap 160 Front

Aleve Gelcap 160 Front
Aleve Gelcaps 220 mg naproxen sodium coated tablets in a blue and red label featuring the Aleve brand name prominently. The label specifies 160 gelatin-coated capsule-shaped tablets, highlights the product as an NSAID pain reliever and fever reducer, and notes strength lasting 12 hours. Bayer HealthCare LLC is indicated as the labeler.*
FDA Label Image

C6896d47 Fa1d 8d72 E053 2a95a90a0acc

C6896d47 Fa1d 8d72 E053 2a95a90a0acc
Aleve Gelcaps 220 mg naproxen sodium coated tablets package label by Bayer HealthCare LLC. The label highlights 'Easy Open Arthritis Cap' and 'All Day Strong' with 160 gelatin coated capsule-shaped tablets. It states pain reliever/fever reducer and notes the package is not child-resistant. The Bayer logo is visible at the bottom.*

* 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.