- Active ingredient (in each tablet)
- Purpose
- Uses
-
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.
When using this product
- drowsiness may occur
- alcohol, sedatives, and tranquilizers may increase drowsiness
- avoid alcoholic drinks
- 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.
-
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
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Compare to Zyrtec® active ingredient††
ORIGINAL PRESCRIPTION STRENGTH
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
TABLETS
††This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Zyrtec®.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
walgreens.com
- Package Labeling
-
INGREDIENTS AND APPEARANCE
WAL-ZYR
cetirizine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0606 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) Product Characteristics Color WHITE Score 2 pieces Shape OVAL Size 9mm Flavor Imprint Code G;4 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0606-14 14 in 1 CARTON 08/31/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0363-0606-05 5 in 1 CARTON 08/31/2018 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:0363-0606-30 1 in 1 BOX 08/31/2018 3 300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:0363-0606-45 1 in 1 BOX 08/31/2018 4 45 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 5 NDC:0363-0606-03 1 in 1 BOX 08/31/2018 5 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA209274 08/31/2018 Labeler - Walgreens (008965063)