Loratadine Allergy Relief
- Dosage form
- TABLET
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Label updated
- 2026-03-19
- 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 useif you have ever had an allergic reaction to this product or any of its ingredients.
Label information
Ask a doctor before use if you haveliver or kidney disease. Your doctor should determine if you need a different dose.
Label information
When using this productdo not take more than directed. Taking more than directed may cause drowsiness.
Label information
Stop use and ask a doctor ifan 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 SEAL IS BROKEN OR MISSING FROM BOTTLE..
Inactive ingredients
corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch
Questions?
call 1-800-406-7984
PRINCIPAL DISPLAY PANEL - 10 mg Tablet
[Image in the official label — see DailyMed source]
DailyMed Set ID: 7127b39d-3686-4249-b720-43c02b4c4654 · Version 19
NDC: 55289-728