Label: SINULIEF- loratadine tablet
- NDC Code(s): 85510-101-01
- Packager: RoseWell Pharmaceuticals LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 9, 2025
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- Official Label (Printer Friendly)
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Active Ingredient (in each tablet)Loratadine 10 mg.....................................................................................................Antihistamine
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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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WHEN USINGAdults and children 6 years and older 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 ...
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Other information
store between 20° to 25°C (68°-77° F) protect from excessive moisture - do not use if blister unit is torn or open - retain carton for complete product information.
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Innactive ingredients
lactose monohydrate, magnesium stearate, pregelatinized starch, sodium starch glycolate.
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Questions and Comments?
Call 1-833-999-7795
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PURPOSETemporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose - itchy, watery eyes - sneezing - itching of the nose or throat - Temporarily relieves these ...
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Package Label.Principal Display Panel
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INGREDIENTS AND APPEARANCEProduct Information
