Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 55301-291-03, 55301-291-06, 55301-291-12, 55301-291-14
  • Packager: ARMY AND AIR FORCE EXCHANGE SERVICE
  • 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: menstrual cramps - toothache - backache - the common cold - headache - 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
    store between 20º-25ºC (68º-77ºF) avoid excessive heat 40ºC (104ºF) see end flap for expiration date and lot number
  • 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
    exchange ✓ select™ Compare To The Active Ingredient - of Advil® Tablets†  Ibuprofen - IBUPROFEN Tablets USP, 200 mg  - Pain Reliever/Fever Reducer (NSAID) 100 Coated Tablets - Tablets - Actual ...
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