LORATADINE- loratadine tablet

Country: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ixtrih issa

Ingredjent attiv:

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

Disponibbli minn:

Northstar RxLLC

INN (Isem Internazzjonali):

LORATADINE

Kompożizzjoni:

LORATADINE 10 mg

Rotta amministrattiva:

ORAL

Tip ta 'preskrizzjoni:

OTC DRUG

Indikazzjonijiet terapewtiċi:

Antihistamine Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

L-istatus ta 'awtorizzazzjoni:

Abbreviated New Drug Application

Karatteristiċi tal-prodott

                                LORATADINE- LORATADINE TABLET
NORTHSTAR RXLLC
----------
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:
•
•
•
•
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
runny nose
itchy, watery eyes
sneezing
itching of the nose or throat
OTHER INFORMATION
•
•
•
INACTIVE INGREDIENTS
Lactose monohydrate, magnesium stearate, microcrystalline cellulose
and sodium starch glycolate.
QUESTIONS OR COMMENTS?
1-800-206-7821
© 2005 NORTHSTAR HEALTHCARE HOLDINGS I10-2015M
Manufactured for: Northstar Rx LLC
Memphis, TN 38141.
Manufactured by: Sandoz Inc.
Princeton, NJ 08540.
10 MG LABEL
NDC 16714-482-01
Non-Drowsy*
Loratadine
Tablets, USP
10 mg
Antihistamine
Indoor & Outdoor Allergies
30 Tablets
NORTHSTAR™
24 Hour
Relief of:
Safety sealed: do not use if the imprinted bottle seal is open or torn
(for bottle only).
Safety sealed: do not use if open or torn (for blister package only).
Store at 20° to 25°C (68° to 77°F) (see USP Controlled Room
Temperature).
Sneezing
Runny Nose
Itchy, Watery
Eyes
Itchy Throat
or Nose
LORATADINE
loratadine tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:16 714-48 2
R
                                
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