Walgreens Headache Relief Extra Strength Tablet, Coated
Product Images NDC 0363-6693

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Walgreens Headache Relief Extra Strength (NDC 0363-6693). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreens, 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

Carton (Headache Relief Es 120ct)

Walgreens Headache Relief Extra Strength coated tablets pack label. Each tablet contains Acetaminophen 250 mg, Aspirin 250 mg, and Caffeine 65 mg. The package contains 120 geltab tablets. Label highlights product use as a pain reliever and nonsteroidal anti-inflammatory drug. Manufacturer marked as Walgreens Co.*

FDA Label Image

Carton (Headache Relief Es 20ct)

Walgreens Headache Relief Extra Strength geltabs package label. The coated oral tablets contain Acetaminophen 250 mg, Aspirin 250 mg (NSAID), and Caffeine 65 mg per tablet. The label states the product is produced by Walgreens and comes in a package of 20 geltabs. The label features detailed drug facts including active ingredients, uses, warnings, directions, and storage information on a green background with white and red text.*

FDA Label Image

Carton (Headache Relief Es 80ct)

Walgreens Headache Relief Extra Strength tablet packaging label showing coated tablets containing Acetaminophen 250 mg, Aspirin 250 mg, and Caffeine 65 mg. The label highlights 80 geltabs per bottle, with detailed drug facts including active ingredients, uses, warnings, directions, and inactive ingredients. The labeler is Walgreens, with a green and white design and barcode on the side.*

* 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.