Label: TOPCARE ALL DAY ALLERGY- cetirizine hydrochloride tablet, film coated

  • NDC Code(s): 36800-458-06, 36800-458-13, 36800-458-39, 36800-458-47, view more
    36800-458-58, 36800-458-66, 36800-458-72, 36800-458-75, 36800-458-87, 36800-458-95
  • Packager: Topco Associates LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 29, 2021

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  • Active ingredient (in each tablet)

    Cetirizine HCl 10 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

    adults and children

    6 years and over

    one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.

    adults 65 years and over

    ask a doctor

    children under 6 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 printed foil under cap is broken or missing
  • Inactive ingredients

    corn starch, FD&C blue no. 1 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, polydextrose, polyethylene glycol, povidone, titanium dioxide, triacetin

  • Questions or comments?

    1-888-423-0139

  • Principal Display Panel

    COMPARE TO ZYRTEC® ACTIVE INGREDIENT

    ORIGINAL PRESCRIPTION STRENGTH

    All Day Allergy

    CETIRIZINE HYDROCHLORIDE TABLETS 10 mg - ANTIHISTAMINE

    INDOOR & OUTDOOR ALLERGIES

    24 HOUR

    RELIEF OF:

    ● Sneezing

    ● Runny Nose

    ● Itchy, Watery Eyes

    ● Itchy Throat or Nose

    90 TABLETS 10 mg EACH

    actual size

    4H288-all-day-allergy
  • INGREDIENTS AND APPEARANCE
    TOPCARE ALL DAY ALLERGY 
    cetirizine hydrochloride tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-458
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYDEXTROSE (UNII: VH2XOU12IE)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIACETIN (UNII: XHX3C3X673)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize10mm
    FlavorImprint Code 4H2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:36800-458-135 in 1 CARTON02/12/200812/31/2021
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:36800-458-6614 in 1 CARTON01/10/2008
    21 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:36800-458-391 in 1 CARTON04/16/2009
    330 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:36800-458-951 in 1 CARTON09/08/2009
    445 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:36800-458-721 in 1 CARTON01/28/2008
    560 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:36800-458-751 in 1 CARTON09/19/2008
    690 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:36800-458-471 in 1 CARTON05/26/2010
    7150 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:36800-458-871 in 1 CARTON04/28/2010
    8300 in 1 BOTTLE; Type 0: Not a Combination Product
    9NDC:36800-458-061 in 1 CARTON03/20/2014
    970 in 1 BOTTLE; Type 0: Not a Combination Product
    10NDC:36800-458-581 in 1 CARTON02/05/2014
    1040 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07833601/10/2008
    Labeler - Topco Associates LLC (006935977)
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