Headache Relief Tablet
Product Images NDC 37808-586

2 FDA label images from H E B · 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 Headache Relief (NDC 37808-586). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H E B, 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

Acetaminophen 250 mg, Aspirin 250 mg (nsaid)*, Caffeine 65 mg, *nonsteroidal Anti-inflammatory (Extra Strength Headache Relief Geltab Pat 1)

Acetaminophen 250 mg, Aspirin 250 mg (nsaid)*, Caffeine 65 mg, *nonsteroidal Anti-inflammatory (Extra Strength Headache Relief Geltab Pat 1)
The packaging label for H-E-B Extra Strength Headache Relief tablets features the proprietary name with active ingredients Acetaminophen 250 mg, Aspirin (NSAID) 250 mg, and Caffeine 65 mg. The label states it is a pain reliever and pain reliever aid, contains 20 Geltabs in actual size, and includes a comparison to Excedrin Extra Strength. The label also displays drug facts, warnings, directions, inactive ingredients, and contact information for questions or comments.*
FDA Label Image

Extra Strength Headache Relief Geltab Pat 2

Extra Strength Headache Relief Geltab Pat 2
The label for H-E-B Headache Relief Extra Strength tablets lists active ingredients as acetaminophen 250 mg, aspirin 250 mg, and caffeine 65 mg. It is an oral pain reliever and pain reliever aid packaged as 20 geltabs. The label includes comparison to Excedrin Extra Strength, warnings, directions, and manufacturer information from H-E-B.*

* 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.