WAL-ITIN ALLERGY RELIEF- loratadine solution 
Walgreen Company

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Wal-itin® Allergy Relief

Drug Facts

Active ingredient
(in each 5 mL)

Loratadine 5 mg

Purpose

Antihistamine

Uses

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.
  • side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

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
2 teaspoonfuls daily; do not take
more than 2 teaspoonfuls in 24 hours
children 2 to under
6 years of age
1 teaspoonful daily; do not take more
than 1 teaspoonful in 24 hours
consumers with liver
or kidney disease
ask a doctor

Other information

Inactive ingredients

artificial grape flavor, citric acid monohydrate, glycerin, propylene glycol, purified water, sodium benzoate, sodium metabisulfite, sucrose

Distributed by: Walgreen Co.,
200 Wilmot Rd., Deerfield, IL 60015-4616

PRINCIPAL DISPLAY PANEL - 120 mL Bottle Carton

Compare to Children's
Claritin
†® active ingredient

NDC 0363-2085-08

Walgreens

Ages 2 Years
& Older

24 HOUR
ALLERGY RELIEF

Children's Non-Drowsy*
WAL-ITIN®

Loratadine Oral Solution,
5mg/5mL Antihistamine

Allergy Relief
Alcohol-Free

Relief of:

Dye-Free

Original Prescription Strength

GRAPE
FLAVORED SYRUP

4 FL OZ (120 mL)

* When taken as directed. See Drug Facts Panel.

PRINCIPAL DISPLAY PANEL - 120 mL Bottle Carton
WAL-ITIN ALLERGY RELIEF 
loratadine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2085
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Loratadine (UNII: 7AJO3BO7QN) (Loratadine - UNII:7AJO3BO7QN) Loratadine5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
citric acid monohydrate (UNII: 2968PHW8QP)  
glycerin (UNII: PDC6A3C0OX)  
propylene glycol (UNII: 6DC9Q167V3)  
water (UNII: 059QF0KO0R)  
sodium benzoate (UNII: OJ245FE5EU)  
sodium metabisulfite (UNII: 4VON5FNS3C)  
sucrose (UNII: C151H8M554)  
Product Characteristics
ColorYELLOW (Colorless to slightly yellow) Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-2085-081 in 1 CARTON
1120 mL in 1 BOTTLE
2NDC:0363-2085-011 in 1 CARTON
2240 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07680508/20/2004
Labeler - Walgreen Company (008965063)
Registrant - Taro Pharmaceuticals U.S.A., Inc. (145186370)
Establishment
NameAddressID/FEIBusiness Operations
Taro Pharmaceutical Indutries Ltd.600072078MANUFACTURE(0363-2085)

Revised: 1/2013
Document Id: baec871b-0e97-42ca-88c7-83220512f588
Set id: bb7392d6-77b9-42d3-82d2-8b21715774c8
Version: 2
Effective Time: 20130122
 
Walgreen Company