Label: CETIRIZINE HYDROCHLORIDE (ALLERGY)- cetirizine hydrochloride tablet

  • NDC Code(s): 69842-237-01, 69842-237-09, 69842-237-17, 69842-237-19, view more
    69842-237-23, 69842-237-39, 69842-237-45, 69842-237-54, 69842-237-57, 69842-237-60, 69842-237-91
  • Packager: CVS Pharmacy, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated November 4, 2022

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  • SPL UNCLASSIFIED SECTION


    Drug Facts

  • Active ingredient (in each tablet)


    Cetirizine hydrochloride USP 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° to 25°C (68° to 77°F)
    • TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING.
  • Inactive ingredients

    colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide

  • Questions?

    call 1-855-274-4122
    Distributed by:
    CVS Pharmacy, Inc.
    One CVS Drive,
    Woonsocket, RI 02895
    © 2020 CVS/pharmacy
    CVS.com®
    1-800-SHOP CVS

    Made in India

    Code: TS/DRUGS/19/1993

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container Label)

    CVS

    HealthTM

    NDC 69842-237-09
    Indoor & Outdoor
    Allergies
    Original Prescription Strength
    Allergy Relief
    CETIRIZINE HYDROCHLORIDE
    TABLETS USP 10 mg
    Antihistamine
    24 Hour
    30 TABLETS

    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container Label)

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container Carton Label)

    CVS HealthTM

    Compare to the active

    ingredient in Zyrtec® Tablets*

    Indoor & Outdoor Allergies
    NDC 69842-237-09
    Original Prescription Strength
    Allergy Relief
    CETIRIZINE HYDROCHLORIDE
    TABLETS USP 10 mg
    Antihistamine
    24 Hour

    Relief of:

    • Sneezing
    • Runny nose
    • Itchy, watery eyes
    • Itchy throat or nose

    Actual Bottle Size
    on Side Panel
    Actual Size
    30 TABLETS

    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 mg (30 Tablets Container carton Label)

  • INGREDIENTS AND APPEARANCE
    CETIRIZINE HYDROCHLORIDE (ALLERGY) 
    cetirizine hydrochloride tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-237
    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
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorWHITE (White to Off-white) Scoreno score
    ShapeROUNDSize8mm
    FlavorImprint Code X;36
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-237-911 in 1 CARTON07/26/2019
    130 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:69842-237-091 in 1 CARTON07/26/2019
    230 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:69842-237-171 in 1 CARTON07/26/2019
    345 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:69842-237-541 in 1 CARTON07/26/2019
    470 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:69842-237-191 in 1 CARTON07/26/2019
    590 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:69842-237-231 in 1 CARTON07/26/2019
    6120 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:69842-237-452 in 1 CARTON07/26/2019
    7120 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:69842-237-39365 in 1 BOTTLE; Type 0: Not a Combination Product07/26/2019
    9NDC:69842-237-601 in 1 CARTON07/26/2019
    95 in 1 BLISTER PACK; Type 0: Not a Combination Product
    10NDC:69842-237-571 in 1 CARTON07/26/2019
    105 in 1 BLISTER PACK; Type 0: Not a Combination Product
    11NDC:69842-237-011 in 1 CARTON07/26/2019
    1114 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09076007/26/2019
    Labeler - CVS Pharmacy, Inc. (062312574)
    Registrant - Aurohealth LLC (078728447)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aurobindo Pharma Limited918917642ANALYSIS(69842-237) , MANUFACTURE(69842-237)
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