LORATADINE tablet

국가: 미국

언어: 영어

출처: NLM (National Library of Medicine)

유효 성분:

LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)

제공처:

AvPAK

관리 경로:

ORAL

처방전 유형:

OTC DRUG

치료 징후:

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.

승인 상태:

Abbreviated New Drug Application

제품 특성 요약

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