Label: ADVIL- ibuprofen tablet coated tablet, coated

  • NDC Code(s): 29485-1005-4, 29485-6500-4, 29485-6749-6, 29485-7012-3
  • Packager: Lil' Drug Store Products, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 5, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Drug Facts

    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 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 non-prescription 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

    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 at 20 weeks or later in 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 under 12 years: ask a doctor

  • Other Information

    •read all warnings and directions before use. Keep carton.
    •store at 20-25°C (68-77°F)
    •avoid excessive heat above 40°C (104°F)

  • Inactive Ingredients

    acetylated monoglycerides, colloidal silicon dioxide, corn starch, croscarmellose sodium, methylparaben, microcrystalline cellulose, pharmaceutical glaze, pharmaceutical ink, povidone, pregelatinized starch, propylparaben, sodium benzoate, sodium lauryl sulfate, stearic acid, sucrose, synthetic iron oxide, titanium dioxide, white wax

  • Questions or comments?

    call toll free 1-800-88-ADVIL

  • SPL UNCLASSIFIED SECTION

    Repackaged and distributed with permission of GSK Consumer Healthcare by:
    Convenience Valet®, Glendale Heights, IL 60139

  • PRINCIPAL DISPLAY PANEL

    Advil

    Ibuprofen Tablets, 200mg

    Pain Reliever/Fever Reducer (NSAID)

    2 Packets of

    2 Coated Tablets Each

    Advil

    Tablets

    Advil 4ct

  • PRINCIPAL DISPLAY PANEL

    Advil

    Ibuprofen Tablets, 200mg

    Pain Reliever/Fever Reducer (NSAID)

    3 Packets of

    2 Coated Tablets Each

    Advil

    Tablets

    Advil 6ct

  • PRINCIPAL DISPLAY PANEL

    Advil

    Ibuprofen Tablets, 200mg

    Pain Reliever/Fever Reducer (NSAID)

    • Headache
    • Minor Pain of Arthritis
    • Toothache
    • Muscular Aches
    • Menstrual Cramps
    • Fever

    30 PACKETS OF 2 COATED TABLETS EACH

    Advil 30ct

  • CVP 4 Count Carton

    Advil

    Ibuprofen Tablets, 200mg

    Pain Reliever/Fever Reducer (NSAID)

    [pill image]

    Tablets

    4

    Coated

    Tablets

    CVP

    HEALTH

    Advil CVP 4ct

  • INGREDIENTS AND APPEARANCE
    ADVIL 
    ibuprofen tablet coated tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29485-1005
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SHELLAC (UNII: 46N107B71O)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SUCROSE (UNII: C151H8M554)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    DIACETYLATED MONOGLYCERIDES (UNII: 5Z17386USF)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorbrownScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code ADVIL
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29485-1005-42 in 1 BLISTER PACK04/30/200211/18/2025
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01898904/30/200211/18/2025
    ADVIL 
    ibuprofen tablet coated tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29485-6749
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SHELLAC (UNII: 46N107B71O)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SUCROSE (UNII: C151H8M554)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    DIACETYLATED MONOGLYCERIDES (UNII: 5Z17386USF)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorbrownScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code ADVIL
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29485-6749-63 in 1 BLISTER PACK02/06/201711/07/2025
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01898902/06/201711/07/2025
    ADVIL 
    ibuprofen tablet coated tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29485-7012
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SHELLAC (UNII: 46N107B71O)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SUCROSE (UNII: C151H8M554)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    DIACETYLATED MONOGLYCERIDES (UNII: 5Z17386USF)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorbrownScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code ADVIL
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29485-7012-330 in 1 BOX11/01/201612/31/2025
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01898911/01/201612/31/2025
    ADVIL 
    ibuprofen tablet coated tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29485-6500
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SHELLAC (UNII: 46N107B71O)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SUCROSE (UNII: C151H8M554)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    DIACETYLATED MONOGLYCERIDES (UNII: 5Z17386USF)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorbrownScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code ADVIL
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29485-6500-42 in 1 BLISTER PACK08/17/201712/31/2025
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01898908/17/201712/31/2025
    Labeler - Lil' Drug Store Products, Inc. (093103646)