SHOPRITE ALLERGY RELIEF- loratadine tablet 
Wakefern Food Corporation

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ShopRite 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 Only}
do not use if printed foil under cap is broken or missing {Bottle Only}
store between 20° to 25°C (68° to 77°F)
protect from excessive moisture {Blister Only}

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-800-SHOPRITE

Principal Display Panel

Compare to: Active Ingredient in Claritin® Tablets

NON-DROWSY†

ORIGINAL PRESCRIPTION STRENGTH

ALLERGY RELIEF

Loratadine Tablets, 10 mg/Antihistamine

INDOOR & OUTDOOR ALLERGIES

24 Hour

Relief of: Sneezing; Runny Nose; Itchy, Water Eyes; Itchy Throat or Nose

actual size

10 Days of Relief

10 tablets

†When taken as directed. See Drug Facts Panel.

ShopRite Allergy Relief
SHOPRITE ALLERGY RELIEF 
loratadine tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:41190-612
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:41190-612-46 10 in 1 CARTON
1 1 in 1 BLISTER PACK
2 NDC:41190-612-72 1 in 1 CARTON
2 60 in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076301 08/06/2013
Labeler - Wakefern Food Corporation (069722418)

Revised: 12/2014
Document Id: faaf3479-667e-4fc4-b220-4166b2c6dcbb
Set id: ba9a2252-4d9c-47b0-a107-6b27ae242301
Version: 2
Effective Time: 20141218
 
Wakefern Food Corporation