Label: IBUPROFEN capsule, liquid filled

  • NDC Code(s): 41163-185-01, 41163-185-02, 41163-185-03, 41163-185-04, view more
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 30, 2025

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • Active ingredient (in each capsule)
    Solubilized ibuprofen equal to - 200 mg ibuprofen (NSAID)* * nonsteroidal anti-inflammatory drug
  • Purpose
    Pain reliever/fever reducer
  • Uses
    temporarily relieves minor aches and pains due to: headache - toothache - backache - menstrual cramps - the common cold - muscular aches - minor pain of arthritis - temporarily reduces ...
  • 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 capsule every 4 to 6 hours while ...
  • Other information
    each capsule contains:   potassium 20 mg - store at 20-25°C (68-77°F) avoid excessive heat above 40°C (104°F) read all warnings and directions before use - retain carton for complete ...
  • Inactive ingredients
    ammonium hydroxide, FD&C green #3, gelatin, iron oxide black, medium chain triglycerides, polyethylene glycol, propylene glycol, potassium hydroxide, purified water, shellac, sorbitan monooleate ...
  • PRINCIPAL DISPLAY PANEL
    EQUALINE - compare to Advil® Liqui-Gels® active ingredient* NDC 41163-185-01 - ibuprofen capsules - 200mg - pain reliever/fever reducer (NSAID) 20 softgels** (**liquid-filled capsules) actual size
  • INGREDIENTS AND APPEARANCE
    Product Information