Label: UP AND UP IBUPROFEN- ibuprofen tablet, film coated

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated April 6, 2020

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

  • Active ingredient (in each tablet)
    Ibuprofen 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug
  • Purposes
    Pain reliever/fever reducer
  • Uses
    • temporarily relieves minor aches and pains due to: • headache - • muscular aches - • minor pain of arthritis - • toothache - • backache - • the common cold - • menstrual cramps - • temporarily reduces ...
  • Warnings
    Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: • hives - • facial swelling - • asthma (wheezing) • shock - • skin ...
  • Directions
    • do not take more than directed - • the smallest effective dose should be used - Adults and children 12 years and older: • take 1 tablet every 4 to 6 hours while symptoms persist - • if pain ...
  • Other information
    • read all warnings and directions before use - • store at 20-25°C (68-77°F) • avoid high humidity and excessive heat above 40°C (104°F)
  • Inactive ingredients
    colloidal silicon dioxide, corn starch, croscarmellose sodium, hypromellose, iron oxide red, iron oxide yellow, microcrystalline cellulose, polyethylene glycol, polysorbate 80, stearic acid ...
  • Questions?
    Call 1-888-547-7400
  • Package/Label Principal Display Panel
    see new warnings - Compare to active ingredient in Advil® Ibuprofen Tablets - ibuprofen tablets 200 mg - pain reliver/fever reducer (NSAID) PACKAGE NOT CHILD-RESISTANT - ACTUAL SIZE - 500 ...
  • INGREDIENTS AND APPEARANCE
    Product Information