Label: GOOD SENSE IBUPROFEN- ibuprofen tablet, film coated

  • NDC Code(s): 0113-0604-02, 0113-0604-52, 0113-0604-62, 0113-0604-71, view more
    0113-0604-76, 0113-0604-78, 0113-0604-82, 0113-0604-90, 0113-0604-93
  • Packager: L. Perrigo Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated December 5, 2019

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

  • Active ingredient (in each tablet)

    Ibuprofen 200 mg (NSAID)*

    *nonsteroidal anti-inflammatory drug

  • Purposes

    Pain reliever/fever reducer

  • Uses

    temporarily relieves minor aches and pains due to:
    headache
    muscular aches
    minor pain of arthritis
    toothache
    backache
    the common cold
    menstrual cramps
    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 reddening
    rash
    blisters

    If an allergic reaction occurs, stop use and seek medical help right away.

    Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chances are higher if you

    are age 60 or older
    have had stomach ulcers or bleeding problems
    take a blood thinning (anticoagulant) or steroid drug
    take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
    have 3 or more alcoholic drinks every day while using this product
    take more or for a longer time than directed

    Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

    Do not use

    if you have ever had an allergic reaction to ibuprofen or any other pain reliever/fever reducer
    right before or after heart surgery

    Ask a doctor before use if

    you have problems or serious side effects from taking pain relievers or fever reducers
    the stomach bleeding warning applies to you
    you have a history of stomach problems, such as heartburn
    you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke
    you are taking a diuretic

    Ask a doctor or pharmacist before use if you are

    taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
    under a doctor’s care for any serious condition
    taking any other drug

    When using this product

    take with food or milk if stomach upset occurs

    Stop use and ask a doctor if

    you experience any of the following signs of stomach bleeding:
    feel faint
    vomit blood
    have bloody or black stools
    have stomach pain that does not get better
    you have symptoms of heart problems or stroke:
    chest pain
    trouble breathing
    weakness in one part or side of body
    slurred speech
    leg swelling
    pain gets worse or lasts more than 10 days
    fever gets worse or lasts more than 3 days
    redness or swelling is present in the painful area
    any new symptoms appear

    If pregnant or breast-feeding,

    ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • Directions

    do not take more than directed
    the smallest effective dose should be used

    adults and children 12 years and older

    take 1 tablet every 4 to 6 hours while symptoms persist
    if pain or fever does not respond to 1 tablet, 2 tablets may be used
    do not exceed 6 tablets in 24 hours, unless directed by a doctor

    children under 12 years

    ask a doctor
  • Other information

    read all warnings and directions before use
    store at 20-25°C (68-77°F)
    avoid high humidity and excessive heat above 40°C (104°F)
    see end panel for lot number and expiration date
  • Inactive ingredients

    colloidal silicon dioxide, corn starch, croscarmellose sodium, hypromellose, iron oxide red, iron oxide yellow, microcrystalline cellulose, polyethylene glycol, polysorbate 80, stearic acid, titanium dioxide

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    Tablets

    See New Warnings

    Ibuprofen Tablets, 200 mg

    Pain Reliever/Fever Reducer (NSAID)

    Actual Size

    BONUS SIZE

    100+20 Tablets FREE

    120 Coated Tablets

    Compare to active ingredient of Advil® Ibuprofen Tablets

    100% SATISFACTION GUARANTEED

    604C2-ibuprofen.jpg
  • INGREDIENTS AND APPEARANCE
    GOOD SENSE IBUPROFEN 
    ibuprofen tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0113-0604
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorBROWNScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code I2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0113-0604-5210 in 1 VIAL; Type 0: Not a Combination Product04/15/1991
    2NDC:0113-0604-621 in 1 CARTON05/04/1992
    224 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:0113-0604-711 in 1 CARTON09/15/1989
    350 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:0113-0604-761 in 1 CARTON06/15/1991
    4120 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:0113-0604-781 in 1 CARTON09/15/1989
    5100 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:0113-0604-90500 in 1 BOTTLE; Type 0: Not a Combination Product01/18/1993
    7NDC:0113-0604-931000 in 1 BOTTLE; Type 0: Not a Combination Product05/31/2007
    8NDC:0113-0604-02550 in 1 BOTTLE; Type 0: Not a Combination Product06/20/2013
    9NDC:0113-0604-822 in 1 CARTON03/02/2011
    9100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07209609/15/1989
    Labeler - L. Perrigo Company (006013346)