FDA Label for Loratadine 10mg
View Indications, Usage & Precautions
Loratadine 10mg Product Label
The following document was submitted to the FDA by the labeler of this product Meijer. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient (In Each Tablet)
Loratadine 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
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.
Directions
adults and 1 tablet daily; not more
than 1 tablet in 24 hours
children 6 years
and over
children under ask a doctor
6 years of age
consumers with ask a doctor
liver or kidney
disease
Other Information
Tamper evident: do not use if imprinted seal under cap, printed with "SEALED FOR YOUR PROTECTION" is missing, open or broken
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?
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