Active Ingredient (In Each Tablet)
Loratadine 10 mg
The following Structured Product Label (SPL) was submitted to the FDA by Savings Distributors Llc for the product Claritin (NDC 73097-005). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, do not use, ask a doctor before use if you have, when using this product, stop use and ask a doctor, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Loratadine 10 mg
Antihistamine
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
if you have ever had an allergic reaction to this product or any of its ingredients.
liver or kidney disease.
Your doctor should determine if you need a different dose.
do not take more than directed. Taking more than directed may cause drowsiness.
if an allergic reaction to this product occurs. Seek medical help right away.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
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
● safety sealed: do not use if the individual blister unit imprinted with Claritin ® is open or torn
● store between 20° to 25°C (68° to 77°F)
● protect from excessive moisture
corn starch, lactose monohydrate, magnesium stearate
1-800-CLARITIN (1-800-252-7484) or www.claritin.com
* Please review the disclaimer below.