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US · Over-the-counter medicine

allergy relief

Dosage form
TABLET
Labeler
Novartsi Consumer Health, Inc.
Label updated
2009-12-01
Retrieved
2026-09-07
Active ingredients
LORATADINE
View original label and images on DailyMed ↗
Active ingredient

loratadine 10mg

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

Do Not Use

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

Ask Doctor

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

When Using

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

Stop Use

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

Pregnancy or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep Out of Reach of Children

Keep out of reach of children.

Overdose

In case of overdose, get medical help or contact a Poison Control Center right away.

Other Information
  • safety sealed: do not use if the imprinted bottle seal with “sealed for your protection” is open or torn (for bottle carton only)
  • safety sealed: do not use if the imprinted blister unit is open or torn (for blister carton only)
  • store at 20-25°C (68-77°F) (see USP Controlled Room Temperature)
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
Inactive ingredients

lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions

call 1-800-452-0051

 

 Distributed by DOLGENCORP, LLC

100 Mission Ridge

Goodlettsville, TN 37072

Principal Display

[Image in the official label — see DailyMed source]

DailyMed Set ID: 6f8c55ff-124b-4e91-893d-5e7c5663b60b · Version 1
NDC: 0067-6122