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Allergy Relief

Dosage form
TABLET
Labeler
AAA PHARMACEUTICAL, INC.
Label updated
2022-04-21
Retrieved
2026-09-07
Active ingredients
LORATADINE
View original label and images on DailyMed ↗
Label information

Drug Facts

Active ingredient (in each tablet)

Loratadine 10 mg

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
주의사항

Warnings

Label information

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Label information

Ask a doctor before use if you have liver or kidney disease.  Your doctor should determine if you need a different dose.

Label information

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Label information

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

Label information

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).

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
  • store between 20 to 25°C (68 to 77°F)
  • retain carton for complete product information and warnings
Inactive ingredients

lactose monohydrate, magnesium stearate, pregelatinized starch (maize), sodium starch glycolate

PRINCIPAL DISPLAY PANEL

Restore U

NDC 57344-193-17

24 hour

Non-Drowsy*

†Compare to the active ingredient in Claritin® Tablets

Allergy Relief

Loratadine Tablets, 10 mg

Antihistamine

Indoor and Outdoor Allergies

Original Prescription Strength

*When taken as directed. See Drug Facts Panel.

Actual Size

30 TABLETS

[Image in the official label — see DailyMed source]

DailyMed Set ID: 9c8535e3-6a60-4640-b37e-a2260936d9af · Version 3
NDC: 57344-193