Low Dose Aspirin Tablet, Coated
Product Images NDC 79903-481

View Photos of 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 Low Dose Aspirin (NDC 79903-481). 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

Aspirin-250s-label- (Aspirin 250s Label)

Aspirin-250s-label- (Aspirin 250s Label)
Low Dose Aspirin 81 mg Delayed-Release Tablets, pain reliever NSAID by Walmart Inc. The label shows a bottle containing 250 enteric coated tablets. It includes product warnings, uses, and directions. The label emphasizes NSAID classification and delayed-release properties for pain relief.*
FDA Label Image

Aspirin-2x250-ifc (Aspirin 2x250 Ifc)

Aspirin-2x250-ifc (Aspirin 2x250 Ifc)
Low Dose Aspirin 81 mg Delayed-Release Tablets by Equate are coated oral tablets indicated as a NSAID pain reliever. The packaging shows a 2-pack containing two bottles of 250 tablets each, distributed by Walmart Inc. The label highlights safety coating, aspirin regimen, and includes standard drug facts and warnings.*
FDA Label Image

Aspirin-500s-label (Aspirin 500s Label)

Aspirin-500s-label (Aspirin 500s Label)
Drug Facts label for Low Dose Aspirin 81 mg Delayed-Release Tablets, pain reliever (NSAID) by Walmart Inc. Includes purpose, active ingredient, uses, warnings, directions, other information, inactive ingredients, and questions or comments contact information. The label details indications for use, storage instructions, and cautions including allergic reactions and warnings for pregnant or breastfeeding women.*

* 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.