LORATADINE
- Dosage form
- TABLET
- Labeler
- NuCare Pharmaceuticals,Inc.
- Label updated
- 2023-07-13
- Retrieved
- 2026-09-07
- Active ingredients
- LORATADINE
ACTIVE INGREDIENT(S)
Loratadine 10 mg
PURPOSE
Antihistamine
USE(S)
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
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)
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
- Tamper-evident: do not use if foil seal under cap, printed with "SEALED for YOUR PROTECTION" is missing, open or broken
STORAGE
- store between 20° to 25°C (68° to 77°F)
INACTIVE INGREDIENTS
Lactose monohydrate, magnesium stearate, sodium starch glycolate and starch maize pregelatinized
QUESTIONS OR COMMENTS
Contact 1-888-588-1418 Mon-Fri 8:00 AM EST to 5:00 PM EST
PRINCIPAL DISPLAY PANEL
[Image in the official label — see DailyMed source]
DailyMed Set ID: f98ebe1f-c3cc-ce98-e053-6394a90aeb0b · Version 3
NDC: 68071-2971