WAL-ZYR- wal-zyr tablet
Walgreen Company

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Drug Facts

Active ingredients (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 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 one10 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 liveror kidney disease	ask a doctor

Other information

do not use if blister unit is broken or torn
store between 20°C to 25°C (68°F to 77°F)

Inactive ingredients

Lactose monohydrate, microcrystalline cellulose, starch (corn), magnesium stearate, hypromellose, polydextrose, polyethylene glycol, and titanium dioxide

Questions

1-800-706-5575

* This product is not manufactured or distributed by McNeil-PPC, Inc., distributor ofZyrtec®.

Principal Display Panel - 10 mg-Bottle-label-45count

OTC Medicine

Walgreens

Wal-ZyrTM

NDC# 0363-1024-04

24 Hour Allergy

Antihistamine

24 hour symptom relief

45 TABLETS 10 mg each

10 mg-Bottle-label-45count

Principal Display Panel - 10 mg-Carton-label-45count

OTC Medicine

Walgreens

Wal-ZyrTM

Carton

NDC# 0363-1024-04

24 Hour Allergy

Antihistamine

24 hour symptom relief

45 TABLETS 10 mg each

10 mg-Carton-label-45count

WAL-ZYR
wal-zyr tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-1024
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
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
STARCH, CORN (UNII: O8232NY3SJ)
MAGNESIUM STEARATE (UNII: 70097M6I30)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POLYDEXTROSE (UNII: VH2XOU12IE)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
CARNAUBA WAX (UNII: R12CBM0EIZ)

Product Characteristics
Color	WHITE	Score	no score
Shape	RECTANGLE	Size	9mm
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-1024-04	1 in 1 CARTON	09/02/2014	04/30/2021
1		45 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:0363-1024-07	1 in 1 CARTON	09/02/2014	04/30/2021
2		70 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:0363-1024-01	1 in 1 CARTON	09/02/2014	04/30/2021
3		150 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC:0363-1024-03	1 in 1 CARTON	09/02/2014	04/30/2021
4		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	ANDA078317	09/02/2014	04/30/2021

Labeler - Walgreen Company (008965063)

Registrant - Apotex Inc. (209429182)

Name	Address	ID/FEI	Business Operations
Establishment
Apotex Inc.		209429182	manufacture(0363-1024) , analysis(0363-1024)

Revised: 6/2019

Document Id: 942ccf47-65c1-c355-dbbf-54a724886ffe

Set id: ee124853-3cf0-8154-31d8-7caf5965d709

Version: 3

Effective Time: 20190612

Walgreen Company