Label: LORATADINE ANTIHISTAMINE- loratadine tablet
- NDC Code(s): 50090-0836-0, 50090-0836-1, 50090-0836-3, 50090-0836-4, view more
- Packager: A-S Medication Solutions
- This is a repackaged label.
- Source NDC Code(s): 45802-650
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 16, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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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HOW SUPPLIEDProduct: 50090-0836 - NDC: 50090-0836-0 10 TABLET in a BOTTLE - NDC: 50090-0836-4 30 TABLET in a BOTTLE - NDC: 50090-0836-5 90 TABLET in a BOTTLE
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Loratadine
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INGREDIENTS AND APPEARANCEProduct Information