DailyMed - UP AND UP ALLERGY RELIEF- loratadine tablet

NDC Code(s): 11673-612-03, 11673-612-46, 11673-612-58, 11673-612-65, view more
11673-612-72, 11673-612-76, 11673-612-78, 11673-612-82, 11673-612-87, 11673-612-95
Packager: Target Corporation

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None
Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated March 28, 2025

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Active ingredient (in each tablet)
Loratadine 10 mg

Loratadine 10 mg
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Purpose
Antihistamine

Antihistamine
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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

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

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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 ...

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)

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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 ...

Other information
• do not use if printed foil under cap is broken or missing - • store between 20° to 25°C (68° to 77°F)

•

do not use if printed foil under cap is broken or missing

•

store between 20° to 25°C (68° to 77°F)

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Inactive ingredients
lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch
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Questions?
Call 1-888-547-7400

Call 1-888-547-7400
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Principal Display Panel
Compare to active ingredient in Claritin® Original Prescription Strength - Non-Drowsy* Allergy Relief - Loratadine Tablets, 10 mg - Antihistamine - 30 Days of Relief - • Indoor and outdoor allergies - ...

Compare to active ingredient in Claritin®

Original Prescription Strength

Non-Drowsy*

Allergy Relief

Loratadine Tablets, 10 mg

Antihistamine

30 Days of Relief

• Indoor and outdoor allergies

• 24-hour relief of sneezing; runny nose; itchy, watery eyes; itchy throat or nose

24 Hour

up&up™

Actual Size

30 Tablets

30 TABLETS

*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

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INGREDIENTS AND APPEARANCE

Product Information

UP AND UP ALLERGY RELIEF loratadine tablet

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

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

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11673-612-46	10 in 1 CARTON	03/26/2012	04/30/2025
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	08/01/2016
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	10/31/2023
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA076301	03/26/2012

Labeler - Target Corporation (006961700)

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Published Date (What is this?)	Version	Files
Mar 31, 2025	9 (current)	download
Nov 8, 2019	8	download
Mar 30, 2017	7	download
Dec 31, 2015	6	download
Apr 13, 2015	5	download
Mar 26, 2015	4	download
Dec 30, 2014	3	download
Nov 8, 2013	2	download
Sep 17, 2012	1	download

	RxCUI	RxNorm NAME	RxTTY
1	311372	loratadine 10 MG 24HR Oral Tablet	PSN
2	311372	loratadine 10 MG Oral Tablet	SCD
3	311372	loratadine 10 MG 24 HR Oral Tablet	SY

Label: UP AND UP ALLERGY RELIEF- loratadine tablet

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Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

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

	NDC
1	11673-612-03
2	11673-612-46
3	11673-612-58
4	11673-612-65
5	11673-612-72
6	11673-612-76
7	11673-612-78
8	11673-612-82
9	11673-612-87
10	11673-612-95

Label: UP AND UP ALLERGY RELIEF- loratadine tablet

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

UP AND UP ALLERGY RELIEF- loratadine tablet

Number of versions: 9

UP AND UP ALLERGY RELIEF- loratadine tablet

UP AND UP ALLERGY RELIEF- loratadine tablet

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UP AND UP ALLERGY RELIEF- loratadine tablet

If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.