Land: Bandaríkin
Tungumál: enska
Heimild: NLM (National Library of Medicine)
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)
NCS HealthCare of KY, Inc dba Vangard Labs
LORATADINE
LORATADINE 10 mg
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
Abbreviated New Drug Application
LORATADINE- LORATADINE TABLET NCS HEALTHCARE OF KY, INC DBA VANGARD LABS ---------- DRUG FACTS ACTIVE INGREDIENT (IN EACH TABLET) Loratadine, USP 10 mg PURPOS E Antihistamine US ES 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 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 kidney disease ask a doctor OTHER INFORMATION Safety sealed: do not use if the imprinted bottle seal is open or torn. Store at 20º - 25ºC (68º - 77ºF) (see USP Controlled Room Temperature).. INACTIVE INGREDIENTS Lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate. QUESTIONS OR COMMENTS? 1-800-525-8747 03-2008M Sandoz Inc. Princeton, NJ 08540 PRINCIPAL DISPLAY PANEL Loratadine Tablets, USP 10mg LORATADINE loratadine tablet PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:0 6 15-558 6 (NDC:0 78 1-50 77) 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) NCS HealthCare of KY, Inc dba Vangard Labs MAGNESIUM STEARATE (UNII: Lestu allt skjalið