Label: ZYRTEC ALLERGY- cetirizine hydrochloride tablet, film coated

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated January 23, 2025

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  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • 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 ...
  • Directions
    adults and children 6 years and overone 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 ...
  • Other information
    store between 20° to 25°C (68° to 77°F) do not use if clamshell is opened, or if foil inner seal imprinted with "ZYRTEC®" is broken or missing - meets USP Dissolution Test 2
  • Inactive ingredients
    colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide
  • Questions?
    call - 1-800-343-7805 (toll-free) or - 215-273-8755 (collect)
  • PRINCIPAL DISPLAY PANEL
    Original Prescription Strength - NDC 50580-726-36 - ZYRTEC - ® ALLERGY - Cetirizine HCl tablets - 10 mg /antihistamine ...
  • INGREDIENTS AND APPEARANCE
    Product Information