Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 11822-0393-1, 11822-0393-2, 11822-0393-4, 11822-0393-5
  • Packager: Rite Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated April 14, 2025

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  • Active ingredient (in each orange caplet)
    Ibuprofen USP, 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug
  • Purpose
    Pain reliever/fever reducer
  • Uses
    temporarily relieves minor aches and pains due to: backache - muscular aches - toothache - menstrual cramps - headache - the common cold - 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: shock - facial swelling - blisters - rash - hives - skin reddening - asthma ...
  • Directions
    do not take more than directed - the smallest effective dose should be used - adults and children 12 years and over: take 1 caplet every 4 to 6 hours while symptoms persist - if pain or fever does ...
  • Other information
    store between 20°-25°C (68°-77°F) avoid excessive heat 40°C (104°F) see end flap for expiration date and lot number
  • Inactive ingredients
    carnauba wax, colloidal silicon dioxide, corn starch, FD&C yellow #6 aluminum lake, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene ...
  • Questions or comments?
    Call 1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday
  • Principal Display Panel
    NDC 11822-0393-5 - Compare to the - active ingredient in - Motrin® IB Caplets† PAIN RELIEF - IBUPROFEN - IBUPROFEN TABLETS USP, 200 mg - PAIN RELIEVER/FEVER REDUCER - (NSAID) ACTUAL ...
  • INGREDIENTS AND APPEARANCE
    Product Information