Label: SUNMARK CHILDRENS LORATADINE SRP SF GRAPE- loratadine solution
- NDC Code(s): 70677-0029-1
- Packager: Strategic Sourcing Services LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 19, 2024
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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 useif you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you haveliver 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 informationdo not use if bottle wrap imprinted with "SEALED FOR SAFETY" is broken or missing. see bottom panel for lot number and expiration date - store between 20° and 25°C (68° and 77°F)
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Inactive ingredientsbutylated hydroxyanisole, glycerin, grape flavor, maltitol solution, masking agent, phosphoric acid, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium phosphate ...
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Questions?Call - 1-866-923-4914
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SPL UNCLASSIFIED SECTIONDistributed by McKesson - One Post Street, San Francisco, CA 94104
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PRINCIPAL DISPLAY PANEL - 120 mL Bottle Cartonsunmark - ® Original - Prescription - Strength - COMPARE TO - CHILDREN'S CLARITIN - ® ACTIVE INGREDIENT* NDC 70677-0029-1 - children's - Allergy - Loratadine Oral ...
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INGREDIENTS AND APPEARANCEProduct Information
