Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 50844-257-15
  • Packager: L.N.K. International, Inc.
  • 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: menstrual cramps - toothache - the common cold - backache - 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: shock - skin reddening - asthma (wheezing) rash - facial ...
  • 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 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, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium ...
  • Questions or comments?
    1-844-428-2538
  • Principal Display Panel
    24/7 life - BY 7-ELEVEN™ Ibuprofen - Ibuprofen Tablets USP, 200 mg - Pain Reliever/Fever Reducer (NSAID) compare to - ADVIL® TABLETS - active ingredient** 50 - TABLETS - Actual ...
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