UP AND UP ALLERGY RELIEF- loratadine tablet

up and up allergy relief by

Drug Labeling and Warnings

up and up allergy relief by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

INGREDIENTS AND APPEARANCE

UP AND UP ALLERGY RELIEF 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-612
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POVIDONE (UNII: FZ989GH94E)

Product Characteristics
Color	WHITE	Score	no score
Shape	OVAL	Size	8mm
Flavor		Imprint Code	L612
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-612-46	10 in 1 CARTON	03/26/2012
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 11673-612-65	1 in 1 CARTON	04/12/2012
2		30 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 11673-612-72	1 in 1 CARTON	04/16/2012	07/01/2016
3		60 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 11673-612-76	1 in 1 CARTON	04/12/2012	02/01/2016
4		120 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 11673-612-82	1 in 1 CARTON	04/12/2012
5		200 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 11673-612-95	1 in 1 CARTON	02/27/2013	02/27/2013
6		45 in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC: 11673-612-03	1 in 1 CARTON	02/19/2015
7		70 in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC: 11673-612-78	100 in 1 BOTTLE; Type 0: Not a Combination Product	03/20/2015
9	NDC: 11673-612-58	1 in 1 CARTON	03/25/2015
9		40 in 1 BOTTLE; Type 0: Not a Combination Product
10	NDC: 11673-612-87	1 in 1 CARTON	03/15/2016
10		300 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA076301	03/26/2012

Labeler - Target Corporation (006961700)