Label: IBUPROFEN 200MG tablet

  • NDC Code(s): 69168-467-03, 69168-467-05, 69168-467-32
  • Packager: Allegiant Health
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated September 30, 2024

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  • Active ingredient(s)
    Ibuprofen USP, 200mg (NSAID)* *nonsteroidal anti-inflammatory drug
  • Purpose
    Pain Reliever/Fever reducer
  • Use(s)
    temporarily relieves minor aches and - pains due to: headache - toothache - backache - menstrual cramps - 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: hives - facial swelling - asthma (wheezing) shock - 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 not ...
  • Other information
    store between 20-25 °C (68-77° F)  read all warnings and directions before use - do not use if seal under bottle cap is broken or missing
  • Inactive ingredients
    Colloidal Silicon Dioxide, Croscarmellose Sodium, FD&C - Blue #2, FD&C Yellow #5, FD&C Yellow #6, Iron Oxide Red, Lecithin, Magnesium - Stearate, Microcrystalline Cellulose, Polyethylene Glycol ...
  • Questions/Comments
    Call 1-888-952-0050 Monday through Friday 9AM – 5PM EST
  • Principal Display Panel
    Ibuprofen
  • INGREDIENTS AND APPEARANCE
    Product Information