Label: LORATADINE tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 50090-0838-0, 50090-0838-1, 50090-0838-3, 50090-0838-4, view more - Packager: A-S Medication Solutions
- This is a repackaged label.
- Source NDC Code(s): 60505-0147
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated January 18, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active ingredient (in each tablet)
Loratadine 10 mg
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Purpose
Antihistamine
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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
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Warnings
Do 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 ...
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Directions
adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours - children under 6 years of ageask a doctor - consumers with liver or kidney diseaseask a ...
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Other information
safety sealed: do not use if induction seal, with "Lift N Peel" tab, under cap is broken or missing - store between 2°C and 30°C (36°F and 86°F) protect from excessive moisture
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Inactive ingredients
colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate, magnesium stearate, microcrystalline cellulose
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HOW SUPPLIEDProduct: 50090-0838 - NDC: 50090-0838-0 10 TABLET in a BOTTLE - NDC: 50090-0838-1 20 TABLET in a BOTTLE - NDC: 50090-0838-3 15 TABLET in a BOTTLE - NDC: 50090-0838-4 30 TABLET in a ...
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Questions or comments?
Call 1-800-706-5575, weekdays, 8:30 am - 5:00 pm Eastern Standard Time - Manufactured by:Manufactured for: Apotex Inc.Apotex Corp. Toronto, OntarioWeston, Florida - Canada M9L ...
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Loratadine
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INGREDIENTS AND APPEARANCEProduct Information