Label: LORATADINE- loratadine solution
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Contains inactivated NDC Code(s)
NDC Code(s): 17856-6234-2, 17856-6234-5 - Packager: Atlantic Biologicals Corps
- This is a repackaged label.
- Source NDC Code(s): 0904-6234
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated August 16, 2016
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENTActive Ingredient: Loratadine 5 mg (in each 5 mL(teaspoonful)(TSP))
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PURPOSEPurpose: Antihistamine
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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 ...
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Warningsever had allergic reaction to this product or any of it's ingredients - Do not use if you have - liver or kidney disease. Your doctor should determine if you need a ...
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Directionsadults and children 6 years and over - 2 teaspoonfuls (TSP) daily; do not take more than 2 teaspoonfuls (TSP) in 24 hours ...
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Other information: sodium 1 mg - Each teaspoonful contains - Safety Sealed. Do not use if imprinted seal around cap is broken or missing - Store between 20° to 25°C (68° to 77°F)
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Inactive ingredientsButylated hydroxylanisole, citric acid, glycerin, grape flavor, propylene glycol, purified water, sodium benzoate, sucralose.
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Questions1-800-616-2471 - Distributed by: Major Pharmaceuticals 31778 Enterprise Drive, Livonia, MI 48150 USA
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LORATADINE SOLUTION(What is this?)
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INGREDIENTS AND APPEARANCEProduct Information