Страна: Соединенные Штаты
Язык: английский
Источник: NLM (National Library of Medicine)
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)
PD-Rx Pharmaceuticals, Inc.
ORAL
OTC DRUG
Antihistamine temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: - runny nose - itchy, watery eyes - sneezing - itching of the nose or throat
Loratadine tablets, 10 mg are supplied as white, film-coated, round biconvex tablets, debossed with “RX526”. In bottles of 10: (NDC 55289-728-10) In bottles of 15: (NDC 55289-728-15) In bottles of 20: (NDC 55289-728-20) In bottles of 30: (NDC 55289-728-30) In bottles of 60: (NDC 55289-728-60) In bottles of 90: (NDC 55289-728-90)
Abbreviated New Drug Application
LORATADINE ALLERGY RELIEF- LORATADINE TABLET PD-RX PHARMACEUTICALS, INC. ---------- LORATADINE ALLERGY RELIEF _DRUG FACTS_ ACTIVE INGREDIENT (IN EACH TABLET) Loratadine, USP 10 mg PURPOSE Antihistamine USES temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat WARNINGS DO 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 if you need a different dose. WHEN USING THIS PRODUCTdo not take more than directed. Taking more than directed may cause drowsiness. STOP USE AND ASK A DOCTOR IFan 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 (1-800-222-1222). DIRECTIONS adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of ask a doctor age ask a doctor consumers with liver or kidney disease ask a doctor OTHER INFORMATION store between 20° to 25° C (68° to 77° F) protect from excessive moisture TAMPER EVIDENT: DO NOT USE IF SEAL IS BROKEN OR MISSING FROM BOTTLE.. INACTIVE INGREDIENTS corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch QUESTIONS? call 1-800-406-7984 PRINCIPAL DISPLAY PANEL - 10 MG TABLET LORATADINE ALLERGY RELIEF loratadine tablet PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:55289-728(NDC:51660-526) ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH STARCH, CORN (UNII: O8232NY3SJ) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) PRODUCT CHARACTERISTICS COLOR white Прочитать полный документ