ALLERGY RELIEF- loratadine tablet 
Novartis Consumer Health, Inc.

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Drug Facts

Active ingredient

loratadine 10mg

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

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask Doctor

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

When Using

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Stop Use

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

Pregnancy or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep Out of Reach of Children

Keep out of reach of children.

Overdose

In case of overdose, get medical help or contact a Poison Control Center right away.

Other Information

Directions

adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Inactive ingredients

lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions

call 1-800-452-0051

 

 Distributed by:

CVS Pharmacy, Inc.

One CVS Drive

Woonsocket, RI 02895

copyright 2009 CVS/pharmacy.

www.cvs.com

1-800-SHOP-CVS

Principal Display

CVS Allergy Relief

CVS

ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-6066
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize6mm
FlavorImprint Code GG;296
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0067-6066-051 in 1 CARTON
15 in 1 BLISTER PACK
2NDC:0067-6066-102 in 1 CARTON
25 in 1 BLISTER PACK
3NDC:0067-6066-202 in 1 CARTON
310 in 1 BLISTER PACK
4NDC:0067-6066-303 in 1 CARTON
410 in 1 BLISTER PACK
5NDC:0067-6066-721 in 1 CARTON
5120 in 1 BOTTLE
6NDC:0067-6066-851 in 1 CARTON
6365 in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA07520901/04/2010
Labeler - Novartis Consumer Health, Inc. (879821635)

Revised: 12/2009
Document Id: 7a2f0eef-7803-497d-926c-a6163a89eb56
Set id: 7a2f0eef-7803-497d-926c-a6163a89eb56
Version: 1
Effective Time: 20091201
 
Novartis Consumer Health, Inc.