LORATADINE- loratadine tablet

País: Estados Unidos

Idioma: inglés

Fuente: NLM (National Library of Medicine)

Ingredientes activos:

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

Disponible desde:

Camber Consumer Care Inc

Vía de administración:

ORAL

tipo de receta:

OTC DRUG

indicaciones terapéuticas:

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 you have 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.

Estado de Autorización:

Abbreviated New Drug Application

Ficha técnica

LORATADINE - LORATADINE TABLET
CAMBER CONSUMER CARE INC
----------
LORATADINE TABLETS, 10 MG
ACTIVE INGREDIENT(S)
Loratadine 10 mg
PURPOSE
Antihistamine
USE(S)
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. (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 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
STORAGE
store between 20° to 25°C (68° to 77°F)
INACTIVE INGREDIENTS
Lactose monohydrate, magnesium stearate, sodium starch glycolate and
starch maize
pregelatinized
QUESTIONS OR COMMENTS
Contact 1-888-588-1418 Mon-Fri 8:00 AM EST to 5:00 PM EST
PRINCIPAL DISPLAY PANEL
LORATADINE 10 MG 100-COUNT CARTON LABEL
LORATADINE 10 MG 100-COUNT CONTAINER LABEL
LORATADINE 10 MG 300-COUNT CONTAINER LABEL
LORATADINE
loratadine tablet
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:69230-328
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 (UNI