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Loratadine Oral

OTC Oral RxCUI 692783
Contents

Overview

Active ingredient
Loratadine
Route
Oral
Label date
2023-09-26

Indications and usage

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

Purpose

Antihistamine

Dosage and administration

Directions use only with enclosed dosing cup adults and children 6 years and over 2 teaspoonfuls (tsp) daily; do not take more than 2 teaspoonfuls (tsp) in 24 hours children 2 to under 6 years of age 1 teaspoonful (tsp) daily; do not take more than 1 teaspoonful (tsp) in 24 hours children under 2 years of age ask a doctor consumers with liver or kidney disease ask a doctor

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

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

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

Stop use and ask a doctor if

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.

Active ingredient (label)

Drug Facts Active ingredient (in each 5 mL teaspoonful) Loratadine USP 5 mg

Inactive ingredients

s artificial flavors, ascorbic acid, glycerin, maltitol, monobasic sodium phosphate monohydrate, phosphoric acid, propylene glycol, purified water, sodium benzoate, sodium metabisulfite, sorbitol, sucralose.

Storage and handling

Other information each teaspoonful contains : sodium 6 mg do not use if carton is opened, or if cap safety seal is broken or missing. store at 20° to 25°C (68° to 77°F)

Keep out of reach of children

of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.