Label: ALL DAY ALLERGY RELIEF- cetirizine hcl tablet
- NDC Code(s): 59726-806-05, 59726-806-14
- Packager: P & L Development, LLC
- Category: HUMAN OTC DRUG LABEL
Updated December 5, 2019
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- Active ingredient (in each tablet)
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.
If pregnant or breast-feeding:
- if breast-feeding: not recommended
- if pregnant: ask a health professional before use
adults and children 6 years and over Take 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 the active ingredient in Zyrtec®*
all day allergy relief
cetirizine HCl 10 mg
treats indoor & outdoor allergies
original prescription strength
24 hour relief of:
- itchy, watery eyes
- runny nose
- itchy throat or nose
*This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Zyrtec®.
TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
200 Hicks Street
Westbury, NY 11590
- Package Labeling
INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY RELIEF
cetirizine hcl tablet
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59726-806 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:59726-806-05 5 in 1 CARTON 06/30/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:59726-806-14 14 in 1 CARTON 06/30/2018 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA209274 06/30/2018 Labeler - P & L Development, LLC (800014821)