Label: UP AND UP CHILDRENS IBUPROFEN- ibuprofen suspension

  • NDC Code(s): 11673-166-26, 11673-166-28, 11673-166-34
  • Packager: Target Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated October 18, 2017

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

  • Active ingredient (in each 5 mL)

    Ibuprofen 100 mg (NSAID)*

    *nonsteroidal anti-inflammatory drug

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  • Purposes

    Pain reliever/fever reducer

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  • Uses

    temporarily:

    relieves minor aches and pains due to the common cold, flu, sore throat, headache and toothache
    reduces fever
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  • 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 your child:

    has had stomach ulcers or bleeding problems
    takes a blood thinning (anticoagulant) or steroid drug
    takes other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
    takes 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.

    Sore throat warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by doctor.

    Do not use

    if the child has 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

    stomach bleeding warning applies to your child
    child has a history of stomach problems, such as heartburn
    child has problems or serious side effects from taking pain relievers or fever reducers
    child has not been drinking fluids
    child has lost a lot of fluid due to vomiting or diarrhea
    child has high blood pressure, heart disease, liver cirrhosis, kidney disease, or had a stroke
    child has asthma
    child is taking a diuretic

    Ask a doctor or pharmacist before use if the child is

    under a doctor’s care for any serious condition
    taking any other drug

    When using this product

    give with food or milk if stomach upset occurs

    Stop use and ask a doctor if

    child experiences any of the following signs of stomach bleeding:
    feels faint
    vomits blood
    has bloody or black stools
    has stomach pain that does not get better
    child has symptoms of heart problems or stroke:
    chest pain
    trouble breathing
    weakness in one part or side of body
    slurred speech
    leg swelling
    the child does not get any relief within first day (24 hours) of treatment
    fever or pain gets worse or lasts more than 3 days
    redness or swelling is present in the painful area
    any new symptoms appear

    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)

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  • Directions

    this product does not contain directions or complete warnings for adult use
    do not give more than directed
    shake well before using
    mL = milliliter
    find right dose on chart. If possible, use weight to dose; otherwise use age.
    use only enclosed dosing cup. Do not use any other dosing device.
    if needed, repeat dose every 6-8 hours
    do not use more than 4 times a day
    replace original bottle cap to maintain child resistance
    wash dosage cup after each use
     
    Dosing Chart

    Weight (lb)

    Age (yr)

    Dose (mL)**

    under 24 lbs

    under 2 years

    ask a doctor

    24-35 lbs

    2-3 years

    5 mL

    36-47 lbs

    4-5 years

    7.5 mL

    48-59 lbs

    6-8 years

    10 mL

    60-71 lbs

    9-10 years

    12.5 mL

    72-95 lbs

    11 years

    15 mL

    **or as directed by a doctor

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  • Other information

    each 5 mL contains: sodium 2 mg
    do not use if printed neckband is broken or missing
    store at 20-25 °C (68-77 °F)
    do not freeze
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  • Inactive ingredients

    anhydrous citric acid, FD&C red #40, glycerin, high fructose corn syrup, hypromellose, natural and artificial bubblegum flavors, polysorbate 80, purified water, sodium benzoate, sorbitol solution, xanthan gum

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  • Questions?

    Call 1-888-547-7400

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  • Principal Display Panel

    see new warnings

    Compare to active ingredient in Children’s Motrin® Bubble Gum Flavor

    children’s ibuprofen

    oral suspension

    100 mg per 5 mL

    pain reliever/fever reducer (NSAID)

    alcohol free

    LASTS UP TO 8 HOURS

    BUBBLEGUM FLAVOR

    AGES 2 TO 11 YEARS

    4 FL OZ (118 mL)

    166UW-childrens-ibuprofen.jpg
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  • INGREDIENTS AND APPEARANCE
    UP AND UP CHILDRENS IBUPROFEN 
    ibuprofen suspension
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-166
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 100 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color PINK (light) Score     
    Shape Size
    Flavor BUBBLE GUM Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-166-26 1 in 1 CARTON 06/12/2009
    1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2 NDC:11673-166-28 1 in 1 CARTON 08/24/2012 12/15/2014
    2 148 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3 NDC:11673-166-34 1 in 1 CARTON 02/19/2013
    3 237 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA074937 06/12/2009
    Labeler - Target Corporation (006961700)
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