Label: LORATADINE tablet
- NDC Code(s): 0904-6852-07, 0904-6852-60, 0904-6852-72, 0904-6852-89
- Packager: Major Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated March 28, 2025
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- Official Label (Printer Friendly)
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Active ingredient (in each tablet)Loratadine 10 mg
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PurposeAntihistamine
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Usestemporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose - • itchy, watery eyes - • sneezing - • itching of the nose or throat
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WarningsDo 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 ...
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Directionsadults 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 ...
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Other information• do not use if printed foil under cap is broken or missing - • store between 20° to 25°C (68° to 77°F)
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Inactive ingredientslactose monohydrate, magnesium stearate, povidone, pregelatinized starch
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Questions or comments? 1-800-719-9260
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Principal Display Panel MAJOR® COMPARE TO the active ingredient of CLARITIN® Non-Drowsy* Original Prescription Strength - Loratadine Tablets, 10 mg/Antihistamine - *When taken as directed. See Drug Facts Panel. Indoor ...
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INGREDIENTS AND APPEARANCEProduct Information
