Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 63981-291-03, 63981-291-14
  • Packager: COSTCO WHOLESALE CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated April 16, 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: backache - menstrual cramps - toothache - headache - the common cold - muscular aches - 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 - 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
    use by expiration date on package - 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
    KIRKLAND - Signature - COMPARE TO - ADVIL® active ingredient** NDC 63981-291-14 - ITM. / ART. 808082 - IBUPROFEN - Tablets USP, 200 mg - Pain Reliever/Fever Reducer (NSAID) Actual ...
  • INGREDIENTS AND APPEARANCE
    Product Information