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

  • NDC Code(s): 0113-9458-04, 0113-9458-13, 0113-9458-39, 0113-9458-58, view more
    0113-9458-66, 0113-9458-75, 0113-9458-88, 0113-9458-95
  • Packager: L. Perrigo Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 11, 2023

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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

    •
    do not use if printed foil under cap is broken or missing
    •
    store between 20 to 25°C (68 to 77°F)
  • 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?

    1-800-719-9260

  • Principal Display Panel

    Allergy

    Original Prescription Strength

    All Day Allergy

    Cetirizine Hydrochloride Tablets, 10 mg Antihistamine

    Actual Size

    24 Hour Relief of:

    • Sneezing

    • Runny Nose

    • Itchy, Watery Eyes

    • Itchy Throat or Nose

    Indoor & Outdoor Allergies

    Compare to active ingredient of Zyrtec®

    30 Tablets

    4H2-c2-all-day-allergy
  • INGREDIENTS AND APPEARANCE
    GOOD SENSE ALL DAY ALLERGY 
    cetirizine hydrochloride tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0113-9458
    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:0113-9458-135 in 1 CARTON01/30/2008
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:0113-9458-6614 in 1 CARTON01/16/2008
    21 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:0113-9458-951 in 1 CARTON04/08/2010
    345 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:0113-9458-391 in 1 CARTON10/28/2008
    430 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:0113-9458-881 in 1 CARTON02/16/201102/16/2011
    530 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:0113-9458-581 in 1 CARTON03/19/201509/01/2016
    640 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:0113-9458-045 in 1 VIAL; Type 0: Not a Combination Product02/16/201102/16/2011
    8NDC:0113-9458-751 in 1 CARTON05/10/2023
    890 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07833601/16/2008
    Labeler - L. Perrigo Company (006013346)
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