Label: QUALITY CHOICE CHILDRENS ALLERGY RELIEF- loratadine solution
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Contains inactivated NDC Code(s)
NDC Code(s): 63868-092-08 - Packager: Chain Drug Marketing Association, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated March 21, 2014
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active ingredient (in each 5 mL teaspoonful)Loratadine 5 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 ...
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Directionsuse only with enclosed dosing cup - adults and children 6 years and over2 teaspoonfuls (tsp) daily; do not take more than 2 teaspoonfuls (tsp) in 24 hours - children 2 to under 6 years of ...
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Other informationsafety sealed: do not use if imprinted safety seal is torn or missing - store between 20° and 25°C (68° and 77°F)
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Inactive ingredientsglycerin, grape flavor, maltitol solution, masking agent, noncrystallizing sorbitol solution, phosphoric acid, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium ...
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Questions?Call 248-449-9300
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SPL UNCLASSIFIED SECTIONDistributed by C.D.M.A., Inc. 43157 W. Nine Mile - Novi, MI 48376-0995
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PRINCIPAL DISPLAY PANEL - 120 mL Bottle CartonNDC 63868-092-08 - QC - QUALITY - CHOICE® Compare to the - active ingredient in - Children's CLARITIN®* children's - Allergy - Relief - Loratadine - Oral Solution 5 mg/5 mL - Antihistamine - Indoor ...
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INGREDIENTS AND APPEARANCEProduct Information
