Label: UP AND UP CHILDRENS ALLERGY- loratadine solution
- NDC Code(s): 82442-207-26
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated July 31, 2024
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- Official Label (Printer Friendly)
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Active ingredient (in each 5 mL teaspoonful) Loratadine 5 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 - • itchy, watery eyes - • sneezing - • 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 determine if ...
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Directions • use only with enclosed dosing cup - adults and children 6 years and over - 2 teaspoonfuls (tsp) daily; do not take more than 2 teaspoonfuls (tsp) in 24 hours - children 2 to under 6 years ...
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Other information • do not use if carton is opened, or if printed neckband is broken or missing - • store between 20° to 25°C (68° to 77°F)
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Inactive ingredients edetate disodium, glycerin, maltitol, monobasic sodium phosphate, natural and artificial grape flavor, phosphoric acid, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose
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Questions or comments? 1-888-547-7400
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Package/Label Principal Display Panel Compare to active ingredient in Children’s Claritin® For Ages 2+ Years Dye & Sugar Free - Children’s Allergy - Loratadine Oral Solution - 5 mg/5 mL - Antihistamine - • Non-drowsy** • Indoor and outdoor ...
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INGREDIENTS AND APPEARANCEProduct Information
