Label: IBUPROFEN tablet, film coated

  • NDC Code(s): 71141-178-22, 71141-178-32
  • Packager: Lidl US LLC
  • 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: headache - backache - toothache - the common cold - muscular aches - menstrual cramps - 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: 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 ...
  • Other information
    store between 20°-25°C (68°-77°F) avoid excessive heat 40°C (104°F) use by expiration date on package
  • 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
    †Compare to the active - ingredient in - Advil® Tablets - NDC 71141-178-22 - Actual Size - 100 - COATED - TABLETS - Ibuprofen - TABLETS USP, 200 mg - PAIN RELIEVER/FEVER REDUCER (NSAID) by LiDL® TAMPER ...
  • INGREDIENTS AND APPEARANCE
    Product Information