Label: LORATADINE capsule, liquid filled
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Contains inactivated NDC Code(s)
NDC Code(s): 41226-686-30 - Packager: KROGER COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 16, 2018
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- Official Label (Printer Friendly)
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ACTIVE INGREDIENTLORATADINE 10MG
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WARNINGSDO NOT USE IF YOU HAVE EVER HAD AN ALLERGIC REACTION TO THIS PRODUCT OR ANY OF ITS INGREDIENTS. WHEN USING THIS PRODUCT DO NOT TAKE MORE THAN DIRECTED. TAKING MORE THAN DIRECTED MAY CAUSE ...
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PURPOSEANTIHISTAMINE
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INDICATIONS & USAGETEMPORARILY RELIEVES THESE SYMPTOMS DUE TO HAY FEVER OR OTHR UPPER RESPIRATORY ALLERGIES: RUNNY NOSE - ITCHY, WATERY EYES - SNEEZING - ITCHING OF THE NOSE OR THROAT
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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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DOSAGE & ADMINISTRATIONADULTS AND CHILDREN 6 YEARS AND OVER: 1 CAPSULE DAILY; NOT MORE THAN 1 CAPSULE IN 24 HOURS. CHILDREN UNDER 6 YEARS OF AGE: ASK A DOCTOR. CONSUMERS WITH LIVER OR KIDNEY DISEASE: ASK A DOCTOR.
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STORAGE AND HANDLINGSTORE BETWEEN 20-25 DEGREES CELSIUS (67-77 DEGREES FAHRENHEIT) PROTECT FROM FREEZING
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INACTIVE INGREDIENTFD&C BLUE #1, GELATIN, MONO AND DIGLYCERIDE OF CAPRYLIC/CAPRIC ACID, PHARMACEUTICAL INK, POLYSORBATE 80, POVIDONE, PURIFIED WATER, SORBITOL SORBITAN SOLUTION.
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information