Home > Drugs A-Z > Up and Up childrens acetaminophen

Up and Up childrens acetaminophen (Target Corporation)

Available Formats

Dosage Form Package Information Links
SUSPENSION 1 BOTTLE in 1 CARTON (11673-105-26) > 118 mL in 1 BOTTLE Label Information
SUSPENSION 1 BOTTLE in 1 CARTON (11673-105-28) > 147 mL in 1 BOTTLE Label Information

Complete Up and Up childrens acetaminophen Information

  • Active ingredient (in each 5 mL)

    Acetaminophen 160 mg


  • Purpose

    Pain reliever/fever reducer


  • Uses

    temporarily:

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

  • Warnings

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if your child takes

    • more than 5 doses in 24 hours, which is the maximum daily amount
    • with other drugs containing acetaminophen

    Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

    • skin reddening
    • blisters
    • rash

    If a skin reaction occurs, stop use and seek medical help right away.

    Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

    Do not use
    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • if your child has ever had an allergic reaction to this product or any of its ingredients

    Ask a doctor before use if your child has

    liver disease

    Ask a doctor or pharmacist before use if your child is

    taking the blood thinning drug warfarin

    When using this product

    do not exceed recommended dose (see overdose warning)

    Stop use and ask a doctor if
    • pain gets worse or lasts more than 5 days
    • fever gets worse or lasts more than 3 days
    • new symptoms occur
    • redness or swelling is present

    These could be signs of a serious condition.

    Keep out of reach of children.

    Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical even if you do not notice any signs or symptoms.


  • Directions

    • this product does not contain directions or complete warnings for adult use
    • do not give more than directed (see overdose warning)
    • shake well before using
    • mL = milliliter
    • find right dose on chart below. If possible, use weight to dose; otherwise, use age.
    • remove the child protective cap and squeeze your child’s dose into the dosing cup
    • repeat dose every 4 hours while symptoms last
    • do not give more than 5 times in 24 hours
     
    • Weight (lb)
     
    • Age (yr)
     
    • Dose (mL)*
     
    • under 24
     
    • under 2 years
     
    • ask a doctor
     
    • 24-35
     
    • 2-3 years
     
    • 5 mL
     
    • 36-47
     
    • 4-5 years
     
    • 7.5 mL
     
    • 48-59
     
    • 6-8 years
     
    • 10 mL
     
    • 60-71
     
    • 9-10 years
     
    • 12.5 mL
     
    • 72-95
     
    • 11 years
     
    • 15 mL

    *or as directed by a doctor

    Attention: use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device.


  • Other information

    • each 5 mL contains: sodium 3 mg
    • store at 20-25°C (68-77°F)
    • do not use if printed neckband is broken or missing
    • see bottom panel for lot number and expiration date

  • Inactive ingredients

    anhydrous citric acid, butylparaben, calcium sulfate, carrageenan, D&C red #33, FD&C red #40, flavor, glycerin, high fructose corn syrup, hydroxyethyl cellulose, microcrystalline cellulose and carboxymethylcellulose sodium, propylene glycol, purified water, sodium benzoate, sorbitol solution, tribasic sodium phosphate


  • Questions?

    Call 1-888-547-7400


  • Principal Display Panel

    Compare to active ingredient in Children’s Tylenol® Oral Suspension

    for ages 2 to 11 years

    children’s

    acetaminophen 160 mg per 5 mL

    oral suspension

    fever reducer/pain reliever

    ibuprofen free

    alcohol free

    aspirin free

    BUBBLEGUM FLAVOR

    DOSAGE CUP INCLUDED

    AGES 2-11 YEARS

    4 fl oz (118 mL)

    Up & Up Children's Acetaminophen Image 1
    Up & Up Children's Acetaminophen Image 2

  • INGREDIENTS AND APPEARANCE
    UP AND UP CHILDRENS ACETAMINOPHEN 
    acetaminophen suspension
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-105
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 160 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    CALCIUM SULFATE (UNII: WAT0DDB505)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM PHOSPHATE, TRIBASIC (UNII: A752Q30A6X)  
    Product Characteristics
    Color RED (opaque) Score     
    Shape Size
    Flavor BUBBLE GUM Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-105-26 1 in 1 CARTON
    1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2 NDC:11673-105-28 1 in 1 CARTON
    2 148 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
    OTC monograph not final part343 07/08/2009
    Labeler - Target Corporation (006961700)