ALLERGY RELIEF- loratadine tablet

Country: Amerika Syarikat

Bahasa: Inggeris

Sumber: NLM (National Library of Medicine)

Bahan aktif:

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

Boleh didapati daripada:

First Aid Direct

Laluan pentadbiran:

ORAL

Jenis preskripsi:

OTC DRUG

Tanda-tanda terapeutik:

 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 

Status kebenaran:

Abbreviated New Drug Application

Ciri produk

ALLERGY RELIEF- LORATADINE TABLET
FIRST AID DIRECT
----------
309 - HEALTH A2Z ALLERGY RELIEF
ACTIVE INGREDIENT
Loratadine 10mg
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.
PREGNANCY/BREAS TFEEDING
IF PREGNANT OR BREAST-FEEDING, ask a health professional before use
KEEP OUT OF REACH OF CHILDREN
KEEP OUT OF REACH OF CHILDREN. In case of accidental overdose, contact
a doctor or Poison Control
Center immediately.
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
store between 20° to 25°C (68° to 77°F)
protect from excessive moisture
do not use if blister unit is torn or open
INACTIVE INGREDIENTS
lactose monohydrate, magnesium stearate, microcrystalline cellulose,
sodium starch glycolate
PRINCIPAL DISPLAY PANEL
NON-DROWSY ALLERG Y RELIEF
ALLERGY RELIEF
loratadine tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:53117-40 7
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)
MAGNESIUM STEARATE (UNII: 70 0 9 7M6 I30 )
CELLULO SE, MICRO CRYSTALLINE (UNII: OP1R32D6 1U)
SO DIUM STARCH GLYCO LATE TYPE A CO RN (UNII: AG9 B6 5PV6 B)
PRODUCT CHA