Label: ZYRTEC ALLERGY- cetirizine hydrochloride tablet, film coated
- NDC Code(s): 67296-1484-3
- Packager: RedPharm Drug Inc
- This is a repackaged label.
- Source NDC Code(s): 50580-726
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated January 23, 2025
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active ingredient (in each tablet)Cetirizine HCl 10 mg
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PurposeAntihistamine
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Usestemporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose - sneezing - itchy, watery eyes - itching of the nose or throat
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WarningsDo 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 ...
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Directionsadults 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 ...
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Other informationstore 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
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Inactive ingredientscolloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide
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Questions?call - 1-800-343-7805 (toll-free) or - 215-273-8755 (collect)
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PRINCIPAL DISPLAY PANELOriginal Prescription Strength - NDC 50580-726-36 - ZYRTEC - ® ALLERGY - Cetirizine HCl tablets - 10 mg /antihistamine ...
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INGREDIENTS AND APPEARANCEProduct Information