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Ibuprofen (NASH-FINCH COMPANY)

Available Formats

Dosage Form Package Information Links
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (70253-291-12) > 100 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (70253-291-08) > 24 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 1 BOTTLE, PLASTIC in 1 CARTON (70253-291-15) > 50 TABLET in 1 BOTTLE, PLASTIC Label Information
TABLET 500 TABLET in 1 BOTTLE, PLASTIC (70253-291-14) Label Information

Complete Ibuprofen Information

  • Active ingredient (in each tablet)

    Ibuprofen USP, 200 mg (NSAID)*

    *nonsteroifal anti-inflammatory drug


  • Purpose

     Pain reliever/fever reducer


  • Uses

    • temporarily relieves minor aches and pains due to:
      • headache
      • the common cold
      • toothache
      • muscular aches
      • backaches
      • minor pain of arthritis
      • 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)
    • skin reddening
    • shock
    • rash
    • blisers

    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 chance is higher is you:

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

    Do not use
    • right before or after heart surgery
    • if you have ever had an allergic reaction to any other pain reliever/fever reducer 

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

    Ask a doctor or pharmacist before use if you are
    •  under a doctor's care for any serious condition
    • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
    • taking any other drug

    When using this product
    • take with food or milk if stomach upset occurs
    • the risk of heart attack or stroke may increase if you use more than directed or for longer than directed

    Stop use and ask a doctor if
    •  you experience any of the following signs of stomach bleeding:
      • feel faint
      • have bloody or black stools
      • vomit blood
      • stomach pain that does not get better
    • 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.


  • 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 respond to 1 tablet, 2 tablets may be used
      • do not exceed 6 tablets in 24 hours, unless directed by a doctor
    • children 12 years: ask a doctor

  • Other information

    • store between 20º-25ºC (68º-77ºF)
    • avoid excessive heat 40ºC (104ºF)
    • see end flap for expiration date and lot number

  • Inactive ingredients

    carnauba wax, corn starch, fumed silica gel, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium starch glycolate, stearic acid, titanium dioxide


  • Questions or comments?

     Call 1-800-426-9391 8:30 am-4:00 pm ET, Monday - Friday


  • Principal Display Panel

    Medicines for Body Aches and Pains

    Compare to the Active Ingredient of Advil®â€ 

    Our Family®
    Quality Care Since 1904

    Ibuprofen
    TABLETS USP (NSAID), 200 mg
    Pain Reliever / Fever Reducer

    100 TABLETS

    SAFETY SEALED

    †This product is not manufactured or distributed by Pfizer Consumer Healthcare, owner of the registered trademark Advil® Tablets.

    50844        REV0411E29112

    DISTRIBUTED BY NASH FINCH COMPANY ©2004, 1996
    NFC BRANDS, 7600 FRANCE AVE S, MPLS, MN 55435
    www.ourfamilyfoods.com     NF16293

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

    Our Family 44-291

    Our Family 44-291


  • INGREDIENTS AND APPEARANCE
    IBUPROFEN 
    ibuprofen tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:70253-291
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg
    Inactive Ingredients
    Ingredient Name Strength
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYDEXTROSE (UNII: VH2XOU12IE)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color BROWN Score no score
    Shape ROUND Size 10mm
    Flavor Imprint Code 44;291
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70253-291-12 1 in 1 CARTON 05/24/1988 09/09/2018
    1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2 NDC:70253-291-08 1 in 1 CARTON 05/24/1988 09/09/2018
    2 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3 NDC:70253-291-15 1 in 1 CARTON 05/24/1988 09/09/2018
    3 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4 NDC:70253-291-14 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/24/1988 09/09/2018
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA075010 05/24/1988 09/09/2018
    Labeler - NASH-FINCH COMPANY (006962294)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 038154464 PACK(70253-291)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867894 MANUFACTURE(70253-291)