Label: LORATADINE ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 76420-330-01, 76420-330-03, 76420-330-05, 76420-330-10, view more
- Packager: Asclemed USA, Inc.
- This is a repackaged label.
- Source NDC Code(s): 51660-526
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 19, 2025
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active ingredient (in each tablet)Loratadine, USP 10 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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Directionsadults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours - children under 6 years of ageask a doctor - consumers with liver or kidney diseaseask a ...
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Other Informationstore between 20° to 25° C (68° to 77° F) protect from excessive moisture - TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
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Inactive ingredientscorn starch, lactose monohydrate, magnesium stearate, pregelatinized starch
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Questions?call - 1-800-406-7984
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SPL UNCLASSIFIED SECTIONRelabeled and Repackaged by: Enovachem PHARMACEUTICALS - Torrance, CA 90501
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information