LORATADINE LORATADINE LACTOSE MONOHYDRATE STARCH, CORN MAGNESIUM STEARATE SODIUM STARCH GLYCOLATE TYPE A POTATO LORATADINE LORATADINE White to off white G;10
Drug Facts
Composition & Profile
Identifiers & Packaging
PRINCIPAL DISPLAY PANEL Loratadine 10 mg Bottle Label NDC 68788-8349 Timeline Description automatically generated
- PRINCIPAL DISPLAY PANEL Loratadine 10 mg Bottle Label NDC 68788-8349 Timeline Description automatically generated
Overview
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
Indications & Usage
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
Dosage & Administration
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
Warnings & Precautions
WARNINGS Do not use if you have ever had an allergic reaction to this product or any of its ingredients. OTHER INFORMATION • Tamper-evident: do not use if foil seal under cap, printed with "SEALED for YOUR PROTECTION" is missing, open or broken
Purpose
PURPOSE Antihistamine
When Using
WHEN USING THIS PRODUCT do not take more than directed. Taking more than directed may cause drowsiness.
Stop Use & Ask a Doctor
STOP USE AND ASK A DOCTOR IF an allergic reaction to this product occurs. Seek medical help right away.
Keep Out of Reach of Children
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)
Storage & Handling
STORAGE • store between 20° to 25°C (68° to 77°F)
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