Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameLORATADINE
Labeler / manufacturerRite Aid Corporation
RouteORAL
Drug classDrug class not supplied in source label
Product NDC11822-0558
Label effective date2026-09-04
Official product label reference
loratadine — Rite Aid Corporation
This page contains 14 source sections for LORATADINE, oral route. Label set 7b804f66-9323-4119-a856-1e6f08280781, version 5.
Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.
Uses described in the label
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
Purpose
Purpose Antihistamine
Dosage and administration — label text
Directions • place 1 tablet on tongue; tablet disintegrates, with or without water 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
Table text from source:
| 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
Warnings
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).
Active ingredient
Active ingredient (in each tablet) Loratadine 10 mg
Do not use
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Ask a doctor before use
Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.
While using this medicine
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
When to stop use and seek help
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.
Child safety
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).
Other safety information
Other information • do not use if printed blister unit is broken or torn • store between 20° to 25°C (68° to 77°F) • use tablet immediately after opening individual blister
Inactive ingredient
Inactive ingredients croscarmellose sodium, crospovidone, hypromellose, magnesium stearate, mannitol, microcrystalline cellulose, natural and artificial mint flavor, sucralose
The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.