Land: USA
Språk: engelska
Källa: NLM (National Library of Medicine)
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)
Lake Erie Medical DBA Quality Care Products LLC
LORATADINE
LORATADINE 10 mg
ORAL
OTC DRUG
Antihistamine temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: - runny nose - sneezing - itchy, watery eyes - itching of the nose or throat
Abbreviated New Drug Application
LORATADINE ANTIHISTAMINE- LORATADINE TABLET LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC ---------- PERRIGO LORATADINE TABLETS, 10 MG DRUG FACTS ACTIVE INGREDIENT (IN EACH TABLET) Loratadine 10 mg PURPOS E Antihistamine US ES temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat WARNINGS DO NOT USE if you have ever had an allergic reaction to this product or any of its ingredients ASK A DOCTOR BEFORE USE IF YOU HAVE liver or kidney disease. Your doctor should determine if you need a different dose. WHEN USING THIS PRODUCT do not take more than directed. Taking more than directed may cause drowsiness. STOP USE AND ASK A DOCTOR IF an allergic reaction to this product occurs. Seek medical help right away. IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away. DIRECTIONS adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or ask a doctor kidney disease OTHER INFORMATION do not use if printed foil under cap is broken or missing store at 20°-25°C (68°-77°F) INACTIVE INGREDIENTS lactose monohydrate, magnesium stearate, povidone, pregelatinized starch QUESTIONS OR COMMENTS? 1-800-719-9260 IMAGE OF LABEL LORATADINE ANTIHISTAMINE loratadine tablet PRODUCT INFORMATION Lake Erie Medical DBA Quality Care Products LLC PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:35356 -8 8 1(NDC:458 0 2-6 50 ) ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH LO RATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH LACTO SE MO NO HYDRATE (UNII: EWQ57Q8 I5X) MAGNESIUM STEARATE (UNII: 70 0 9 7M6 I30 ) PO VIDO NE (UNII: FZ9 8 9 GH9 4E) STARCH, CO RN (UNII: O8 232NY3SJ) PRODUCT Läs hela dokumentet