WAL ZYR- cetirizine hydrochloride tablet, film coated
Walgreen Company

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Walgreen Co. Wal-Zyr™ Drug Facts

Active ingredient (in each tablet)

Cetirizine HCl 10 mg

Purpose

Antihistamine

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

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 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)

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 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

Other information

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

Inactive ingredients

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

Questions or comments?

1-800-719-9260

Principal Display Panel

Walgreens

ORIGINAL PRESCRIPTION STRENGTH

Compare to Zyrtec® active ingredient

Wal-Zyr™

24 HOUR ALLERGY

CETIRIZINE HYDROCHLORIDE TABLETS 10 mg / ANTIHISTAMINE

24 HOUR

TABLETS

INDOOR & OUTDOOR ALLERGIES

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

60 TABLETS 10 mg EACH

24 HOUR

ACTUAL SIZE

WAL ZYR
cetirizine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-0495
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 (UNII: H3R47K3TBD)
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:0363-0495-13	5 in 1 CARTON	01/31/2008	06/30/2023
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:0363-0495-06	1 in 1 CARTON	11/06/2013	11/30/2022
2		70 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:0363-0495-39	1 in 1 CARTON	08/14/2008	09/30/2023
3		30 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC:0363-0495-47	1 in 1 CARTON	05/02/2008	12/31/2023
4		150 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC:0363-0495-66	14 in 1 CARTON	01/09/2008	03/01/2024
5		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
6	NDC:0363-0495-72	1 in 1 CARTON	01/27/2008	02/29/2024
6		60 in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC:0363-0495-75	1 in 1 CARTON	01/27/2008	09/30/2023
7		90 in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC:0363-0495-87	1 in 1 CARTON	01/21/2010	09/30/2023
8		300 in 1 BOTTLE; Type 0: Not a Combination Product
9	NDC:0363-0495-95	1 in 1 CARTON	01/05/2009	11/30/2022
9		45 in 1 BOTTLE; Type 0: Not a Combination Product
10	NDC:0363-0495-58	1 in 1 CARTON	08/08/2016	09/30/2021
10		40 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	01/09/2008	03/01/2024

Labeler - Walgreen Company (008965063)

Revised: 12/2023

Document Id: b8222e44-dd58-41be-aefe-6367ae771a60

Set id: 16625a43-22c1-4754-a7bd-ccc262e2dbd5

Version: 8

Effective Time: 20231207

Walgreen Company