Label: UP AND UP CHILDRENS ALLERGY RELIEF- loratadine solution
- NDC Code(s): 11673-558-26
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 11, 2018
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- Download DRUG LABEL INFO: PDF XML
- 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
- Warnings
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Do not use if you have ever had an allergic reaction to this product or any of its ingredients
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Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.
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When using this product do not take more than directed. Taking more than directed may cause drowsiness.
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Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
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If pregnant or breast feeding, ask a health professional before use.
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Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
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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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Inactive ingredients edetate disodium, glycerin, maltitol, monobasic sodium phosphate, natural and artificial grape flavor, phosphoric acid, propylene glycol, purified water, sodium benzoate, sorbitol ...
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Package/Label Principal Display Panel Compare to active ingredient in Children’s Claritin® dye-free - children’s allergy relief - loratadine oral solution 5 mg/5 mL - antihistamine - indoor and outdoor allergies - non-drowsy* 24-hour relief ...
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INGREDIENTS AND APPEARANCEProduct Information
