Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 11822-0291-0, 11822-0291-1, 11822-0291-2, 11822-0291-3, view more
  • Packager: Rite Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 2, 2025

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  • Active ingredient (in each brown tablet)
    Ibuprofen USP, 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug
  • Purpose
    Pain reliever/fever reducer
  • Uses
    temporarily relieves minor aches and pains due to: muscular aches - headache - menstrual cramps - backache - the common cold - toothache - minor pain of arthritis - temporarily reduces fever
  • Warnings
    Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: facial swelling - shock - hives - asthma (wheezing) skin ...
  • 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 does ...
  • Other information
    see end flap for expiration date and lot number - store between 20°-25°C (68°-77°F) avoid excessive heat 40°C (104°F)
  • Inactive ingredients
    carnauba wax, colloidal silicon dioxide, corn starch, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium ...
  • Questions or comments?
    Call 1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday
  • Principal Display Panel
    TRIAL SIZE - NDC 11822-0291-2 -  Compare to the - active ingredient in - Advil® Tablets** PAIN RELIEF - IBUPROFEN - IBUPROFEN TABLETS USP, 200 mg - PAIN RELIEVER/FEVER REDUCER - (NSAID) ACTUAL ...
  • INGREDIENTS AND APPEARANCE
    Product Information