Active Ingredients And Purpose
Active ingredient (in each tablet)
Cetirizine HCl, 10mg
Purpose
Antihistamine
Cetirizine Hydrochloride Tablets
- Manufacturer
- Sportpharm LLC
- Effective date
- 2026-02-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:37:22
Key Label Information
Uses
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
Warnings
Directions And Dosage
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 Label Information
Other information
store between 20° to 25°C (68° to 77°F)
Inactive ingredients
hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, povidone, starch, titanium dioxide.
Questions?
call 1-888-375-3784 .
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products
- Cetirizine Hydrochloride Tablets
- CETIRIZINE
NDC Codes
Ingredients
Complete SPL Sections
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredient (in each tablet)
Cetirizine HCl, 10mg
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
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)
Inactive ingredients
hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, povidone, starch, titanium dioxide.
Questions?
call 1-888-375-3784 .
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Source Document
Official SPL XML cached by FDA.report · DailyMed PDF
- XML object
- dailymed/d5297bdb-823c-4318-a797-5311d5cf0df8/4a2c3f01-e8a9-c309-e063-6294a90a61e8.xml
- XML SHA-256
- c6216cebebd8fa1128e7263cfa7b7322a39b17d5d9ad72839f13b35b8e63369a
- XML bytes
- 23364
Legacy File Index
| Folder | File | Date |
|---|---|---|
| otc | 4a2c3f01-e8a9-c309-e063-6294a90a61e8.xml | 2026-02-07 |
| otc | 3b5c1ed8-6bc1-c586-e063-6294a90a5a40.xml | 2025-08-08 |
| otc | label.jpg | 2025-08-08 |