Label: CETIRIZINE HYDROCHLORIDE tablet, film coated

  • NDC Code(s): 72789-458-30, 72789-458-51, 72789-458-90
  • Packager: PD-Rx Pharmaceuticals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 29, 2025

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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 ...
  • 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 ...
  • Other information
    store between 20 - 25°C (68 - 77°F) TAMPER EVIDENT: DO NOT USE IF SAFETY SEAL IS BROKEN OR MISSING FROM BOTTLE.
  • Inactive ingredients
    hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, polysorbate, povidone, pregelatinized starch, and titanium dioxide
  • Questions or comments?
    1-613-231-4610 Weekdays 9AM-5PM EST
  • Principal Display Panel
    Cetirizine Hydrochloride Tablets 10 mg - Antihistamine
  • INGREDIENTS AND APPEARANCE
    Product Information
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