LORATADINE ALLERGY RELIEF- loratadine tablet

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

NuCare Pharmaceuticals,Inc.

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

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

Authorization status:

Abbreviated New Drug Application

Summary of Product characteristics

LORATADINE ALLERGY RELIEF- LORATADINE TABLET
NUCARE PHARMACEUTICALS,INC.
----------
DRUG FACTS
ACTIVE INGREDIENT(S)
Loratadine USP, 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.
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 and kidney disease
ask a doctor
OTHER INFORMATION
store between 20 and 25° C (68 and 77° F)
protect from excessive moisture
TAMPER EVIDENT: DO NOT USE IF IMPRINTED 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 -
LORATADINE ALLERGY RELIEF
loratadine tablet
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:68071-5049(NDC:51660-526)
ROUTE OF ADMINISTRATION
ORAL
NuCare Pharmaceuticals,Inc.
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 (White to Off White)
SCORE
no score
SHA