Loratadine
- Dosage form
- TABLET
- Labeler
- Cabinet Health P.B.C.
- Label updated
- 2025-10-27
- Retrieved
- 2026-09-07
- Active ingredients
- LORATADINE
Active ingredient (in each tablet)
Loratadine USP 10 mg
Purpose
Antihistamine
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
• runny nose • itchy, watery eyes • sneezing • 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.
Ask a doctor before use if you have
liver or kidney disease. Your doctor should determine if you need a different dose.
When using this product
do not take more than directed. Taking more than directed may cause drowsiness.
Stop use and ask a doctor if
an allergic reaction to this product occurs. Seek medical help right away.
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
| adults and children 6 years and over | 1 tablet daily; not more than 1 tablet in 24 hours |
| children under 6 years of age | ask a doctor |
| consumers with liver or kidney disease | ask a doctor |
Other information
• Tamper-evident: do not use if foil seal under cap, printed with "SEALED for YOUR PROTECTION" is missing, open or broken
• store between 20° to 25°C (68° to 77°F)
Inactive ingredients
corn starch, lactose monohydrate, magnesium stearate, povidone
Questions or Comments?
Call + 1-908-242-6108
Package Labeling: 82725-0142-1
[Image in the official label — see DailyMed source]
Package Labeling: 82725-0142-3
[Image in the official label — see DailyMed source]
Package Labeling: 82725-0142-4
[Image in the official label — see DailyMed source]
Package Labeling: 82725-0142-2
[Image in the official label — see DailyMed source]
DailyMed Set ID: 8b090fa2-9535-456c-b14d-187a2873cdf7 · Version 1
NDC: 82725-0142