UP AND UP DYE FREE INFANTS CONCENTRATED IBUPROFEN (IBUPROFEN) SUSPENSION/ DROPS [TARGET CORPORATION]

UP AND UP DYE FREE INFANTS CONCENTRATED IBUPROFEN (IBUPROFEN) SUSPENSION/ DROPS [TARGET CORPORATION]
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NDC 11673-255-10, 11673-255-16
Set ID 6cfdcd94-95cb-4447-a14b-cdb49a1e3114
Category HUMAN OTC DRUG LABEL
Packager Target Corporation
Generic Name
Product Class
Product Number
Application Number ANDA075217
  • Active ingredient (in each 1.25 mL)

    Ibuprofen 50 mg (NSAID)*

    *nonsteroidal anti-inflammatory drug

  • Purposes

    Pain reliever/fever reducer

  • Uses

    temporarily:

    reduces fever
    relieves minor aches and pains due to the common cold, flu, sore throat, headaches and toothaches
  • 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

    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)

  • Directions

    this product does not contain directions or complete warnings for adult use
    do not give more than directed
    shake well before using
    find right dose on chart below. If possible, use weight to dose; otherwise use age.
    mL = milliliter
    measure with the dosing device provided. Do not use with any other device.
    dispense liquid slowly into the child’s mouth, toward the inner cheek
    if needed, repeat dose every 6-8 hours
    do not use more than 4 times a day
     
    Dosing Chart

    Weight (lbs)

    Age (mos)

    Dose (mL)

    under 6 mos

    ask a doctor

    12-17 lbs

    6-11 mos

    1.25 mL

    18-23 lbs

    12-23 mos

    1.875 mL

  • Other information

    store at 20-25°C (68-77°F)
    do not freeze
    do not use if printed neckband is broken or missing
  • Inactive ingredients

    anhydrous citric acid, glycerin, hypromellose, natural and artificial berry flavor, polysorbate 80, purified water, sodium benzoate, sorbitol solution, sucrose, xanthan gum

  • Questions?

    Call 1-888-547-7400

  • Principal Display Panel

    see new warnings

    Compare to active ingredient in Motrin® Infants' Drops Dye-Free

    for ages 6 mos. to 23 mos.

    dye-free

    infants'

    concentrated ibuprofen

    oral suspension

    50 mg per 1.25 mL

    pain reliever/fever reducer (NSAID)

    concentrated drops

    non-staining

    LASTS UP TO 8 HOURS

    BERRY FLAVOR

    AGES 6 TO 23 MONTHS

    1 FL OZ (30 mL)

    Use only with enclosed syringe.

    infants conentrated ibuprofen image
  • INGREDIENTS AND APPEARANCE
    UP AND UP DYE FREE INFANTS CONCENTRATED IBUPROFEN 
    ibuprofen suspension/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-255
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN50 mg  in 1.25 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCROSE (UNII: C151H8M554)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorWHITE (Opaque) Score    
    ShapeSize
    FlavorBERRY (mixed) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-255-101 in 1 CARTON07/08/2009
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:11673-255-162 in 1 CARTON08/23/2018
    230 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07521707/08/2009
    Labeler - Target Corporation (006961700)