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Loratadine

Dosage form
TABLET
Labeler
Cabinet Health P.B.C.
Label updated
2025-10-27
Retrieved
2026-09-07
Active ingredients
LORATADINE
View original label and images on DailyMed ↗
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