UP AND UP ALLERGY RELIEF- loratadine tablet 
Target Corporation

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Target Corporation 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 printed foil under cap is broken or missing
store between 20° to 25°C (68° to 77°F)

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions?

Call 1-888-547-7400

Principal Display Panel

CE PACK

Compare to active ingredient in Claritin®

non-drowsy*

allergy relief

loratadine tablets, 10 mg

antihistamine

30 days of relief

original prescription strength

indoor and outdoor allergies

24 hour relief of:

sneezing

runny nose

itchy, watery eyes

itchy throat or nose

24 HOUR

ACTUAL SIZE

30 TABLETS

30 TABLETS

*When taken as directed. See drug facts panel.

allergy relief image
UP AND UP ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-612
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POVIDONE (UNII: FZ989GH94E)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize8mm
FlavorImprint Code L612
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-612-4610 in 1 CARTON03/26/2012
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:11673-612-651 in 1 CARTON04/12/2012
230 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:11673-612-721 in 1 CARTON04/16/201207/01/2016
360 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:11673-612-761 in 1 CARTON04/12/201202/01/2016
4120 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:11673-612-821 in 1 CARTON04/12/2012
5200 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:11673-612-951 in 1 CARTON02/27/201302/27/2013
645 in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:11673-612-031 in 1 CARTON02/19/2015
770 in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:11673-612-78100 in 1 BOTTLE; Type 0: Not a Combination Product03/20/2015
9NDC:11673-612-581 in 1 CARTON03/25/2015
940 in 1 BOTTLE; Type 0: Not a Combination Product
10NDC:11673-612-871 in 1 CARTON03/15/2016
10300 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07630103/26/2012
Labeler - Target Corporation (006961700)

Revised: 10/2019
Document Id: a136b013-3a10-444a-8a58-36af71f0aa72
Set id: c4ef0110-89c3-4ded-9a9a-75c0f794f869
Version: 8
Effective Time: 20191029
 
Target Corporation