Label: IBUPROFEN capsule, liquid filled

  • NDC Code(s): 41226-700-80, 41226-700-87
  • Packager: KROGER COMPANY
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated April 13, 2024

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  • Drug Facts
  • ACTIVE INGREDIENT
    Active ingredient (in each capsule) Solubilized ibuprofen equal to - 200 mg ibuprofen (NSAID)* (present as the free acid and potassium salt) *nonsteroidal anti-inflammatory drug
  • PURPOSE
    Purpose - Pain reliever/Fever reducer
  • INDICATIONS & USAGE
    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 fever
  • WARNINGS
    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 ...
  • DOSAGE & ADMINISTRATION
    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 symptoms persist - if pain ...
  • STORAGE AND HANDLING
    Other information - each capsule contains:potassium 20 mg - read all warnings and directions before use - store at 20-25ºC (68-77ºF) avoid excessive heat above 40°C (104°F).
  • INACTIVE INGREDIENT
    Inactive ingredientsammonium hydroxide, FD&C green no.3, gelatin, iron oxide black, medium chain triglycerides, polyethylene glycol, potassium hydroxide, propylene glycol, purified water, shellac ...
  • QUESTIONS
    Questions or comments? Call - 1-800-632-6900
  • PRINCIPAL DISPLAY PANEL(What is this?)
    ibu-80s-ifc ...
  • INGREDIENTS AND APPEARANCE
    Product Information