Label: TYLENOL EXTRA STRENGTH- acetaminophen tablet, coated

  • NDC Code(s): 50580-490-10, 50580-490-20, 50580-490-24, 50580-490-25, view more
  • Packager: Kenvue Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 27, 2025

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • Active ingredient (in each gelcap)
    Acetaminophen 500 mg
  • Purpose
    Pain reliever/fever reducer
  • Uses
    temporarily relieves minor aches and pains due to: headache - muscular aches - backache - minor pain of arthritis - the common cold - toothache - premenstrual and menstrual ...
  • Warnings
    Liver warning - This product contains acetaminophen. Severe liver damage may occur if you take - more than 4,000 mg of acetaminophen in 24 hours - with other drugs containing acetaminophen - 3 or more ...
  • Directions
    do not take more than directed (see - overdose warning) adults and children 12 years and over - take 2 gelcaps every 6 hours while symptoms last - do not ...
  • Other information
    store between 20-25°C (68-77°F). Avoid high humidity. do not use if carton is opened. Do not use if foil inner seal imprinted with "TYLENOL" is broken or missing
  • Inactive ingredients
    benzyl alcohol, butylparaben, carboxymethylcellulose sodium, D&C yellow no. 10, edetate calcium disodium, FD&C blue no. 1, FD&C red no. 40, gelatin, hypromellose, iron oxide, magnesium stearate ...
  • Questions or comments?
    call - 1-877-895-3665 (toll-free) or - 215-273-8755 (collect)
  • PRINCIPAL DISPLAY PANEL
    NDC 50580-490-24 - Extra Strength - TYLENOL - ® FOR ADULTS - Acetaminophen - Pain Reliever - Fever Reducer - RAPID RELEASE ...
  • INGREDIENTS AND APPEARANCE
    Product Information