allergy relief medication

Dosage form: tablet
Ingredients: LORATADINE 10mg
Labeler: Target Brands, Inc.
NDC Code: 11673-315

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

Adverse Reactions

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
  • safety sealed: do not use if the imprinted bottle seal with “sealed for your protection” is open or torn (for bottle carton only)
  • safety sealed: do not use if the imprinted blister unit is open or torn (for blister carton only)
  • store at 20-25°C (68-77°F) (see USP Controlled Room Temperature)

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 Target Corp.

Minneapolis, MN 55403

copyright 2009 Target Brands, Inc.

All Rights Persevered

Principal Display

Target

ALLERGY RELIEF MEDICATION 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-315
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE 
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize6mm
FlavorImprint CodeGG;296
Contains    
Packaging
#Item CodePackage Description
1NDC:11673-315-102 BLISTER PACK (BLISTER PACK) in 1 CARTON
15 TABLET (TABLET) in 1 BLISTER PACK
2NDC:11673-315-404 BLISTER PACK (BLISTER PACK) in 1 CARTON
210 TABLET (TABLET) in 1 BLISTER PACK
3NDC:11673-315-181 BOTTLE (BOTTLE) in 1 CARTON
3180 TABLET (TABLET) in 1 BOTTLE
4NDC:11673-315-606 BLISTER PACK (BLISTER PACK) in 1 CARTON
410 TABLET (TABLET) in 1 BLISTER PACK
5NDC:11673-315-303 BLISTER PACK (BLISTER PACK) in 1 CARTON
510 TABLET (TABLET) in 1 BLISTER PACK
6NDC:11673-315-153 BLISTER PACK (BLISTER PACK) in 1 CARTON
65 TABLET (TABLET) in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520901/31/2010
Labeler - Target Brands, Inc. (006961700)

Revised: 09/2010
 
Target Brands, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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