Label: IBUPROFEN tablet, coated

  • NDC Code(s): 72476-109-01, 72476-109-02, 72476-109-03, 72476-109-05, view more
  • Packager: RETAIL BUSINESS SERVICES , LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated March 5, 2021

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  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • Active ingredient (in each tablet)
    Ibuprofen 200 mg (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 ...
  • 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 ...
  • Other information
    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 product information and warnings
  • Inactive ingredients
    colloidal silicon dioxide, corn starch, iron oxide red, polyethylene glycol, polyvinyl alcohol, povidone K30, pregelatinized starch, sodium starch glycolate, stearic acid, talc, titanium ...
  • PRINCIPAL DISPLAY PANEL
    CAREONE® NDC 72476-109-01 - Compare to the active ingredient in Advil® Ibuprofen Tablets† IBUPROFEN - Tablets, 200 mg - Pain Reliever / Fever Reducer - (NSAID) Actual Size - 24 TABLETS
  • INGREDIENTS AND APPEARANCE
    Product Information