SOUND BODY ALLERGY RELIEF- loratadine tablet

Summary of Product characteristics

                                SOUND BODY ALLERGY RELIEF- LORATADINE TABLET
BIG LOTS STORES, INC.
----------
BIG LOTS, INC ALLERGY RELIEF DRUG FACTS
ACTIVE INGREDIENT (IN EACH TABLET)
Loratadine 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. (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 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, povidone, pregelatinized
starch
QUESTIONS OR COMMENTS?
1-800-719-9260
PRINCIPAL DISPLAY PANEL
Compare to the Active Ingredient in Claritin Tablets
NON-DROWSY*
Original Prescription Strength
Allergy Relief
Loratadine Tablets, 10 mg
Antihistamine
*When taken as directed. See Drug Facts Panel.
Indoor & Outdoor Allergies
24 HOUR RELIEF OF: Sneezing; Runny Nose;
Itchy, Watery Eyes; Itchy Throat or Nose
30 TABLETS
Actual Size
24 HOUR
do not use if blister unit is broken or torn
store between 20 to 25 C (68 to 77 F)
°
°
°
°
protect from excessive moisture
®
SOUND BODY ALLERGY RELIEF
loratadine tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:50 59 4-0 10
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
                                
                                Read the complete document