Label: CONCENTRATED IBUPROFEN INFANTS- ibuprofen suspension/ drops

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated November 28, 2022

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

  • ACTIVE INGREDIENT (in each 1.25 mL)

    Ibuprofen, USP 50 mg (NSAID)*
    *nonsteroidal anti-inflammatory drug

  • PURPOSE

    Pain reliever/fever reducer

  • USE(S)

    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 you 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

    • take with food or milk if stomach upset occurs
  • STOP USE AND ASK 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 the 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 dosing device provided. Do not use any other dosing 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 (lb) AGE (mos) DOSE (mL) 
     under 6 mos
     
     ask a doctor
    12-17 lbs 6-11 mos 1.25 mL
     18-23 lbs 12-23 years 1.875 mL



  • OTHER INFORMATION

    • store between 20-25oC (68-77oF)
    • do not use if carton is opened or if printed neckband is imprinted with "SEALED FOR YOUR PROTECTION" and "USE WITH ENCLOSED DOSING DEVICE ONLY" is broken or missing.
  • INACTIVE INGREDIENTS

    anhydrous citric acid, flavors, glycerin, polysorbate 80, pregelatinized starch, purified water, sodium benzoate, sorbitol, sucrose, xanthan gum

  • QUESTIONS OR COMMENTS?

    call 1-609-860-2600 (Monday - Friday 8 am - 4 pm)

  • PRINCIPAL DISPLAY PANEL

    NDC 53041-637-09
    See New Warnings

    For Ages 6 mos. to 23 mos.
    Concentrated Infants' Drops
    IBUPROFEN
    Oral Suspension
    50 mg per 1.25 mL
    Pain Reliever/Fever Reducer
    (NSAID)

    Lasts up to 8 Hours
    Dye-Free


    Berry Flavor
    1 fl oz (30 mL)
    GUARDIAN


    637-GDC-1


  • INGREDIENTS AND APPEARANCE
    CONCENTRATED IBUPROFEN INFANTS 
    ibuprofen suspension/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53041-637
    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)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SUCROSE (UNII: C151H8M554)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorBERRY (Mixed Berry) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53041-637-091 in 1 CARTON10/03/2018
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21075510/03/2018
    Labeler - Guardian Drug Company (119210276)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guardian Drug Company119210276MANUFACTURE(53041-637)