ALLERGY RELIEF MEDICATION- loratadine tablet 
Target Corporation

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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

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 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

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

Target

ALLERGY RELIEF MEDICATION 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-315
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
MICROCRYSTALLINE CELLULOSE (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:11673-315-102 in 1 CARTON01/31/201011/30/2014
15 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:11673-315-404 in 1 CARTON01/31/201011/30/2014
210 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:11673-315-181 in 1 CARTON01/31/201011/30/2014
3180 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:11673-315-606 in 1 CARTON01/31/201011/30/2014
410 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:11673-315-303 in 1 CARTON01/31/201011/30/2014
510 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC:11673-315-153 in 1 CARTON01/31/201011/30/2014
65 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520901/31/201011/30/2014
Labeler - Target Corporation (006961700)

Revised: 1/2018
 
Target Corporation