IBUPROFEN TABLET, COATED [HEB]

IBUPROFEN TABLET, COATED [HEB]
PDF | XML

NDC 37808-410-02, 37808-410-05
Set ID c04ad0b4-5d8a-4861-9eaa-b2aaa7b19664
Category HUMAN OTC DRUG LABEL
Packager HEB
Generic Name
Product Class
Product Number
Application Number ANDA079174
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each caplet)

    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 arthritis
    • 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 chance is 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 any other pain reliever/fever reducer
    • right before or after heart surgery

    Ask a doctor before use if

    • stomach bleeding warning applies to you
    • you have problems or serious side effects from taking pain relievers or fever reducers
    • 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

    • 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

    Stop use and ask a doctor if

    ■ side effects occur.  You may report side effects to FDA at 1-800-FDA-1088.

    ■ 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 over: 

       ■ take 1 caplet every 4 to 6 hours while symptoms persist

       ■ if pain or fever does not respond to 1 caplet, 2 caplets may be used

       ■ do not exceed 6 caplets in 24 hours, unless directed by a doctor

    ■ children under 12 years:  ask a doctor

  • 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 dioxide

  • Questions or comments?

    1-844-705-4384

  • PRINCIPAL DISPLAY PANEL

    Compare to Advil® Caplets active ingredient

    NDC 37808-410-02

    HEB

    Ibuprofen Tablets, 200mg

    Pain Reliever/Fever Reducer (NSAID)

    For Body Aches and Pains

    Actual Size

    50 COATED CAPLETS**

    **Capsule-shaped Tablets

    image description

  • INGREDIENTS AND APPEARANCE
    IBUPROFEN 
    ibuprofen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-410
    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)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    POVIDONE K30 (UNII: U725QWY32X)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorbrownScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code G2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37808-410-021 in 1 CARTON01/01/2013
    150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:37808-410-05500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917401/01/2011
    Labeler - HEB (007924756)

Related Drugs