Label: LORATADINE tablet
- NDC Code(s): 60760-831-00
- Packager: ST. MARY'S MEDICAL PARK PHARMACY
- This is a repackaged label.
- Source NDC Code(s): 70010-162
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated January 15, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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ACTIVE INGREDIENT(S)Loratadine 10 mg
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PURPOSEAntihistamine
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USE(S)temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose - sneezing - itchy, water eyes - itching of the nose or ...
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WARNINGSDO 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 IFyou have liver or kidney disease. Your doctor should determine if you need a different dose.
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WHEN USING THIS PRODUCTdo not take more than directed. Taking more than directed may cause drowsiness.
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STOP USE AND ASK DOCTOR IFan allergic reaction to this product occurs. Seek medical help right away.
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PREGNANCY/BREASTFEEDINGask a health professional before use
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KEEP OUT OF REACH OF CHILDRENIn case of overdose, get medical help or contact a Poison Control Center right away.
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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 INFORMATIONTamper-evident: do not use if foil seal under cap, printed with "SEALED for YOUR PROTECTION" is missing, open or broken - Blister Foil Units - safety sealed: do not use if the individual ...
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STORAGEstore between 20º to 25ºC (68º to 77ºF)
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INACTIVE INGREDIENTSLactose monohydrate, magnesium stearate, sodium starch glycolate and starch maize pregelatinized
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QUESTIONS OR COMMENTSContact 1-877-770-3183 Mon-Fri 9:00 AM to 4:30 PM EST.
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information