Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 68210-4201-2
  • Packager: Spirit Pharmaceuticals LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated December 13, 2024

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  • Drug Facts
  • Active Ingredient (in each tablet)
    Ibuprofen 200 mg (NSAID)** **nonsteroidal anti-inflammatory drug
  • Purpose
    Pain reliever/fever reducer
  • Uses
    • temporarily relieves minor aches and pains due to: • headache • toothache • backache - • menstrual cramps • the common cold • muscular aches • minor pain of arthritis • temporarily ...
  • Warnings
    Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: • hives • facial swelling • asthma ...
  • Directions
    • do not take more than directed • the smallest effective dose should be used • adults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persist • if pain or fever ...
  • Other Information
    • read all warnings and directions before use. Keep carton. • store between 20°-25°C (68°-77°F) • avoid excessive heat above 40°C (104°F)
  • Inactive ingredients
    Colloidal silicon dioxide, corn starch, hypromellose, red iron oxide, magnesium stearate*, microcrystalline cellulose*, povidone K-30*, pregelatinized starch, sodium starch glycolate ...
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  • Principal Display 
    Label - Carton
  • INGREDIENTS AND APPEARANCE
    Product Information