SMART SENSE ALLERGY RELIEF NON DROWSY- loratadine tablet 
Kmart Corporation

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Kmart Corporation Allergy Relief Drug Facts

Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

Uses

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. (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

Other information

do not use if blister unit is broken or torn (Blister configuration)
do not use if printed foil under cap is broken or missing (Bottle configuration)
store between 20° to 25°C (68° to 77°F)
protect from excessive moisture

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to the active ingredient of Claritin® Tablets

Original Prescription Strength

Non-Drowsy*

INDOOR & OUTDOOR ALLERGIES

Allergy Relief

Loratadine Tablets, 10 mg/Antihistamine

ACTUAL SIZE

24 HOUR™

Relief of:

Sneezing

Itchy, Watery Eyes

Runny Nose

Itchy Throat or Nose

*When taken as directed. See Drug Facts Panel.

10 TABLETS

Smart Sense Allergy Relief
SMART SENSE ALLERGY RELIEF  NON DROWSY
loratadine tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49738-612
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg
Inactive Ingredients
Ingredient Name Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POVIDONES (UNII: FZ989GH94E)  
Product Characteristics
Color WHITE Score no score
Shape OVAL Size 8mm
Flavor Imprint Code L612
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49738-612-46 10 in 1 CARTON
1 1 in 1 BLISTER PACK
2 NDC:49738-612-39 30 in 1 CARTON
2 1 in 1 BLISTER PACK
3 NDC:49738-612-72 1 in 1 CARTON
3 60 in 1 BOTTLE
4 NDC:49738-612-75 1 in 1 CARTON
4 90 in 1 BOTTLE
5 NDC:49738-612-49 40 in 1 CARTON
5 1 in 1 BLISTER PACK
6 NDC:49738-612-58 1 in 1 CARTON
6 40 in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076301 11/24/2010
Labeler - Kmart Corporation (008965873)

Revised: 12/2014
Document Id: 86572b92-7fb7-4b93-ad68-f7757bdaa7e6
Set id: 970f9b70-2c58-4f06-903c-913d874534ca
Version: 3
Effective Time: 20141229
 
Kmart Corporation