Loratadine ODT
Loratadine ODT is an FDA drug label for the active ingredient LORATADINE manufactured by Better Living Brands, LLC administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230925.
Generic: LORATADINE
Manufacturer: Better Living Brands, LLC
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 21130-221
Application: ANDA208477
Effective: 20230925
Active Ingredients: Active ingredient (in each tablet) Loratadine USP 10 mg
Indications & Usage
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat
Dosage & Administration
Directions place 1 tablet on tongue; tablet disintegrates, with or without water 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
Contraindications
Not available.
Warnings
Warnings
Adverse Reactions
Not available.
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