Loratadine Allergy Relief
- Dosage form
- TABLET
- Labeler
- A-S Medication Solutions
- Label updated
- 2026-02-19
- Retrieved
- 2026-09-07
- Active ingredients
- LORATADINE
Label information
Drug Facts
Active ingredient (in each tablet)
Loratadine, USP 10 mg
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
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.
Label information
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)
- protect from excessive moisture
- TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
Inactive ingredients
corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch
Questions?
call 1-800-406-7984
Label information
Distributed by:
Ohm Laboratories Inc.
New Brunswick, NJ 08901
HOW SUPPLIED
Product: 50090-2387
NDC: 50090-2387-0 30 TABLET in a BLISTER PACK
Loratadine
[Image in the official label — see DailyMed source]
DailyMed Set ID: a53e5635-8633-4c28-b04f-cdfb3d851e68 · Version 13
NDC: 50090-2387