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Loratadine

Dosage form
TABLET
Labeler
Cardinal Health 107, LLC
Label updated
2024-01-19
Retrieved
2026-09-07
Active ingredients
LORATADINE
View original label and images on DailyMed ↗
Active ingredient (in each tablet)

Loratadine 10 mg

Original Prescription Strength

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. (1-800-222-1222)

This unit dose package is not child resistant and is Intended for Institutional Use Only.

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
  • •do not use if printed foil under cap is broken or missing
  • •store between 20° to 25°C (68° to 77°F)
  • •Gluten Free
Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Distributed by:

MAJOR® PHARMACEUTICALS

17177 N Laurel Park Dr., Suite 233

Livonia, MI 48152 USA

Distributed by:
Cardinal Health

Dublin, OH 43017

L5534946-11223

L5534946-21223

Principal Display Panel

Loratadine Tablets

10 mg

Original Prescription Strength

Antihistamine

10 Tablets

[Image in the official label — see DailyMed source]

DailyMed Set ID: 7283a8e9-db56-4fac-aade-95a32fed4494 · Version 3
NDC: 55154-8082