UP AND UP CHILDRENS ALLERGY RELIEF (CETIRIZINE HCL) SOLUTION [TARGET CORPORATION]

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UP AND UP CHILDRENS ALLERGY RELIEF (CETIRIZINE HCL) SOLUTION [TARGET CORPORATION]
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NDC 11673-303-26, 11673-303-34
Set ID a96dd5b9-ff2d-49dc-8eb4-bade8a64bb37
Category HUMAN OTC DRUG LABEL
Packager Target Corporation
Generic Name
Product Class
Product Number
Application Number ANDA204226
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  • Active ingredient (in each 5 mL)

    Cetirizine HCl 5 mg

  • Purpose

    Antihistamine

  • Uses

    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

    •
    runny nose
    •
    sneezing
    •
    itchy, watery eyes
    •
    itching of the nose or throat
  • Warnings

    Do not use

    if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

    Ask a doctor before use if you have

    liver or kidney disease. Your doctor should determine if you need a different dose.

    Ask a doctor or pharmacist before use if you are

    taking tranquilizers or sedatives.

    When using this product

    •
    drowsiness may occur
    •
    avoid alcoholic drinks
    •
    alcohol, sedatives, and tranquilizers may increase drowsiness
    •
    be careful when driving a motor vehicle or operating machinery

    Stop use and ask a doctor if

    an allergic reaction to this product occurs. Seek medical help right away.

    If pregnant or breast-feeding:

    •
    if breast-feeding: not recommended
    •
    if pregnant: ask a health professional before use.
  • 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

    •
    use only with enclosed dosing cup
    •
    find right dose on chart below
    •
    mL = milliliter

    adults and children

    6 years and over

    5 mL or 10 mL once daily depending upon severity of symptoms; do not take more than 10 mL in 24 hours.

    adults 65 years

    and over

    5 mL once daily; do not take more than 5 mL in 24 hours.

    children 2 to under

    6 years of age

    2.5 mL once daily. If needed, dose can be increased to a maximum of 5 mL once daily or 2.5 mL every 12 hours. Do not give more than 5 mL in 24 hours.

    children under

    2 years of age

    ask a doctor

    consumers with liver or kidney disease

    ask a doctor

    Other information

    •
    store between 20°-25°C (68°-77°F)
    •
    do not use if carton is opened, or if printed neckband is broken or missing
    •
    see bottom panel for lot number and expiration date
  • Inactive ingredients

    anhydrous citric acid, artificial bubble gum flavor, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose

    Questions?

    Call 1-888-547-7400

  • Package/Label Principal Display Panel

    Compare to active ingredient in Children’s Zyrtec®

    children’s allergy relief

    cetirizine hydrochloride oral solution 1 mg/mL

    antihistamine

    indoor and outdoor allergies

    24 hour relief of:

    sneezing

    runny nose

    itchy, watery eyes

    itchy throat or nose

    DYE AND SUGAR FREE

    24 HOUR

    dosing cup included

    BUBBLEGUM FLAVOR

    AGES 2+ YEARS

    4 FL OZ (118 mL)

    189-uw-childrens-allergy-relief.jpg
  • INGREDIENTS AND APPEARANCE
    UP AND UP CHILDRENS ALLERGY RELIEF 
    cetirizine hcl solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-303
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorYELLOW (Clear to light yellow) Score    
    ShapeSize
    FlavorBUBBLE GUMImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-303-261 in 1 CARTON03/07/2018
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:11673-303-341 in 1 CARTON03/08/2019
    2236 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20422603/07/2018
    Labeler - Target Corporation (006961700)
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