Ország: Egyesült Államok
Nyelv: angol
Forrás: NLM (National Library of Medicine)
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)
AvPAK
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 liver or kidney disease. Your doctor should determine if you need a different dose. an allergic reaction to this product occurs. Seek medical help right away.
Abbreviated New Drug Application
LORATADINE- LORATADINE TABLET AVPAK ---------- LORATADINE TABLETS USP 10 MG _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 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 (1-800-222- 1222) right away. _DIRECTIONS_ adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor _OTHER INFORMATION_ Tamper-evident: do not use if foil seal under cap, printed with “SEALED for YOUR PROTECTION” is missing, open or broken store at 20° to 25°C (68° to 77°F) protect from excessive moisture _INACTIVE INGREDIENTS_ lactose monohydrate, magnesium stearate, pregelatinized starch (maize), sodium starch glycolate. _QUESTIONS OR COMMENTS?_ call 1-855-361-3993 PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 10 MG (45 TABLETS BOTTLE) LORATADINE loratadine tablet PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:50268-489 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 LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) STARCH, CORN (UN Olvassa el a teljes dokumentumot