LORATADINE ALLERGY RELIEF- loratadine tablet

Šalis: Jungtinės Valstijos

kalba: anglų

Šaltinis: NLM (National Library of Medicine)

Veiklioji medžiaga:

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

Prieinama:

PD-Rx Pharmaceuticals, Inc.

Vartojimo būdas:

ORAL

Recepto tipas:

OTC DRUG

Terapinės indikacijos:

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

Produkto santrauka:

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)

Autorizacija statusas:

Abbreviated New Drug Application

Prekės savybės

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