DailyMed - UP AND UP ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated

NDC Code(s): 11673-502-00, 11673-502-06, 11673-502-39, 11673-502-48, view more
11673-502-58, 11673-502-72, 11673-502-74, 11673-502-75, 11673-502-76, 11673-502-87
Packager: Target Corporation

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

Drug Label Information

Updated March 27, 2025

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Active ingredient (in each tablet)
Cetirizine HCl 10 mg

Cetirizine HCl 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 - • sneezing - • itchy, watery eyes - • itching of the nose or throat

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

•

runny nose

•

sneezing

•

itchy, watery eyes

•

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 or to an antihistamine containing hydroxyzine. Ask a doctor before use if you have - liver or ...

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives.

When using this product

•

drowsiness may occur

•

avoid alcoholic drinks

•

alcohol, sedatives, and tranquilizers may increase drowsiness

•

be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding:

•

if breast-feeding: not recommended

•

if pregnant: 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 - one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms. adults ...

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

•

store between 20-25°C (68-77°F)

•

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

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Inactive ingredients
corn starch, FD&C blue no. 1 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, polydextrose, polyethylene glycol, povidone, titanium dioxide, triacetin

corn starch, FD&C blue no. 1 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, polydextrose, polyethylene glycol, povidone, titanium dioxide, triacetin
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Questions or comments?
1-888-547-7400

1-888-547-7400
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Principal Display Panel
Compare to active ingredient in Zyrtec® Original Prescription Strength - Allergy Relief - Cetirizine Hydrochloride Tablets, 10 mg Antihistamine - • Indoor and outdoor allergies - • 24-hour relief of ...

Compare to active ingredient in Zyrtec®

Original Prescription Strength

Allergy Relief

Cetirizine Hydrochloride Tablets, 10 mg Antihistamine

• Indoor and outdoor allergies

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

24 Hour

Actual Size

60 Tablets

up&up™

60 TABLETS, 10 mg EACH

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INGREDIENTS AND APPEARANCE

Product Information

UP AND UP ALLERGY RELIEF cetirizine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-502
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24)	CETIRIZINE HYDROCHLORIDE	10 mg

Ingredient Name	Strength
Inactive Ingredients
STARCH, CORN (UNII: O8232NY3SJ)
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POLYDEXTROSE (UNII: VH2XOU12IE)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TRIACETIN (UNII: XHX3C3X673)

Product Characteristics
Color	WHITE	Score	no score
Shape	OVAL	Size	10mm
Flavor		Imprint Code	4H2
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11673-502-58	1 in 1 CARTON	02/11/2015	12/31/2023
1		40 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:11673-502-48	2 in 1 CARTON	12/17/2014
2	NDC:11673-502-75	90 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:11673-502-06	1 in 1 CARTON	12/17/2014	10/31/2022
3		70 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC:11673-502-39	1 in 1 CARTON	12/17/2014
4		30 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC:11673-502-74	1 in 1 CARTON	12/17/2014
5		14 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC:11673-502-87	1 in 1 CARTON	03/14/2016
6		300 in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC:11673-502-76	1 in 1 CARTON	10/18/2019
7		120 in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC:11673-502-72	1 in 1 CARTON	01/06/2021
8		60 in 1 BOTTLE; Type 0: Not a Combination Product
9	NDC:11673-502-00	1 in 1 CARTON	03/11/2015
9		90 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	ANDA078336	12/17/2014

Labeler - Target Corporation (006961700)

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Published Date (What is this?)	Version	Files
Mar 31, 2025	9 (current)	download
Aug 14, 2023	8	download
Jun 8, 2023	7	download
Feb 5, 2021	6	download
Oct 22, 2019	5	download
Dec 31, 2015	4	download
Mar 16, 2015	3	download
Jan 13, 2015	2	download
Dec 29, 2014	1	download

	RxCUI	RxNorm NAME	RxTTY
1	1014678	cetirizine HCl 10 MG Oral Tablet	PSN
2	1014678	cetirizine hydrochloride 10 MG Oral Tablet	SCD
3	1014678	cetirizine HCl 10 MG Oral Tablet	SY

Label: UP AND UP ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated

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

Ask a doctor or pharmacist before use if you are

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	one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.
adults 65 years and over	ask a doctor
children under 6 years of age	ask a doctor
consumers with liver or kidney disease	ask a doctor

	NDC
1	11673-502-00
2	11673-502-06
3	11673-502-39
4	11673-502-48
5	11673-502-58
6	11673-502-72
7	11673-502-74
8	11673-502-75
9	11673-502-76
10	11673-502-87

Label: UP AND UP ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated

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

Ask a doctor or pharmacist before use if you are

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- cetirizine hydrochloride tablet, film coated

Number of versions: 9

UP AND UP ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated

UP AND UP ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated

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UP AND UP ALLERGY RELIEF- cetirizine hydrochloride tablet, film coated

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