Label: ASPIRIN LOW DOSE- aspirin tablet, delayed release

  • NDC Code(s): 68016-642-12, 68016-642-40, 68016-642-50
  • Packager: Chain Drug Consortium
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 16, 2025

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  • Active ingredient (in each tablet)
    Aspirin 81 mg (NSAID)* *nonsteroidal anti-inflammatory drug
  • Purpose
    Pain reliever
  • Uses
    for the temporary relief of minor aches and pains or as recommended by your doctor. Because of its delayed action, this product will not provide fast relief of headaches or other symptoms needing ...
  • Warnings
    Reye’s syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea ...
  • Directions
    do not take more than directed - drink a full glass of water with each dose - adults and children 12 years and over: take 4 to 8 tablets every 4 hours not to exceed 48 tablets in 24 hours unless ...
  • Other information
    store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF) use by expiration date on package
  • Inactive ingredients
    corn starch, D&C yellow #10, FD&C yellow #6, hypromellose, methacrylic acid, microcrystalline cellulose, polydextrose, polyethylene glycol, shellac wax, silica, simethicone, sodium bicarbonate ...
  • Questions or comments?
    1-800-426-9391
  • Principal Display Panel
    Premier - Value® †COMPARE TO THE ACTIVE INGREDIENT - IN BAYER® LOW DOSE ASPIRIN - Low Dose - Aspirin 81 mg - PAIN RELIEVER (NSAID) Enteric coated - actual - size - 400 Tablets - TAMPER EVIDENT: DO NOT ...
  • INGREDIENTS AND APPEARANCE
    Product Information