Label: PENTREXCILINA DAY TIME- cetirizine hydrochloride tablet
- NDC Code(s): 69729-137-14
- Packager: OPMX LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 15, 2024
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Drug Facts
Drug Facts
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Active Ingredient
Active Ingredient (in each tablet)Purpose - Cetirizine HCl 10 mgAntihistamine
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Purpose
Antihistamine
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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
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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 ...
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Directions
Adults & Children 6 years and over One 10mg tablet once daily; do not take more than one 10mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms - Adults 65 years and ...
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Other information
tore at room temperature between 20-25°C (68-77°F). close cap tightly after use. contains no ingredients made from a gluten-containing grain (wheat, barley or rye). TAMPER EVIDENT: Do not use if ...
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Inactive ingredients
colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide.
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Questions or comments?
Call (619) 600-5632 - Monday through Friday 9 AM- 5 PM EST
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PRINCIPAL DISPLAY PANELDaytime Xtreme Allergy Relief - Cetirizine HCl 10mg - Non-Drowsy - NDC 69729-137-14 - 14 Tablets - DUO PACK - PENTREXCILINA - ALL DAY & ALL NIGHT - 24 HOUR ALLERGY RELIEF OF: Sneezing/ Estornudos - Runny nose ...
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INGREDIENTS AND APPEARANCEProduct Information