LORATADINE tablet

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

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

Disponível em:

Contract Pharmacy Services-PA

DCI (Denominação Comum Internacional):

LORATADINE

Composição:

LORATADINE 10 mg

Via de administração:

ORAL

Tipo de prescrição:

OTC DRUG

Indicações terapêuticas:

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 de autorização:

Abbreviated New Drug Application

Características técnicas

LORATADINE- LORATADINE TABLET
CONTRACT PHARMACY SERVICES-PA
----------
DRUG FACTS 453
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:
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.
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
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°-25°C (68°-77°F) (see USP Controlled Room
Temperature).
INACTIVE INGREDIENTS
Lactose monohydrate, magnesium stearate, microcrystalline cellulose
and sodium starch glycolate.
QUESTIONS OR COMMENTS?
1-800-525-8747
10-2015M
Sandoz Inc.
Princeton, NJ 08540
10 MG LABEL
NDC 67046-453-30 Non-Drowsy*
Loratadine
Tablets, USP
10 mg
Antihistamine
Indoor & Outdoor Allergies
30 Tablets
SANDOZ
24 Hour
Relief of:
Sneezing
Runny Nose
Itchy, Watery
Eyes
Itchy Throat
or Nose
* When taken as directed.
See Drug Facts Panel.
LORATADINE
loratadine tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 70 46 -453(NDC:0 78 1-50 77)
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGRED