Label: PAIN RELIEF EXTRA STRENGTH- acetaminophen tablet, coated

  • NDC Code(s): 83324-079-50
  • Packager: CHAIN DRUG MARKETING ASSOCIATION, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 13, 2024

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  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • Active ingredient (in each caplet)
    Acetaminophen 500 mg
  • Purpose
    Pain reliever/fever reducer
  • Uses
    temporarily relieves minor aches and pains due to: the common cold - headache - backache - minor pain of arthritis - toothache - muscular aches - premenstrual and menstrual cramps - temporarily ...
  • 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 caplets every 6 hours while symptoms last - swallow whole – do not crush ...
  • Other information
    store between 20-25°C (68-77°F) retain carton for complete product information
  • Inactive ingredients
    acesulfame potassium, flavor, hypromellose, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, sodium starch glycolate, stearic acid, titanium dioxide
  • PRINCIPAL DISPLAY PANEL
    QUALITY CHOICE® NDC 83324-079-50 - †Compare to Active Ingredient in TYLENOL® Extra Strength - For Adults - Extra Strength - Pain Relief - Acetaminophen - Pain Reliever | Fever Reducer - Instant Cooling ...
  • INGREDIENTS AND APPEARANCE
    Product Information