Antihistamines
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Zyrtec Prescribing Information

Drug Detail:Zyrtec (Cetirizine [ se-tir-a-zeen ])

Drug Class: Antihistamines

Contents
Uses Warnings Before Taking Dosage Side effects Interactions FAQ

Drug Facts

ZYRTEC ALLERGY
cetirizine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50580-726
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
Product Characteristics
ColorwhiteScore2 pieces
ShapeRECTANGLE (rounded-off rectangular biconvex tablet) Size9mm
FlavorImprint CodeZYRTEC;10;MG
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50580-726-0350 in 1 CARTON01/01/2008
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:50580-726-133 in 1 CARTON03/21/200901/31/2021
21 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:50580-726-305 in 1 PACKAGE01/01/200811/30/2022
31 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:50580-726-3214 in 1 PACKAGE01/01/200811/30/2022
41 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:50580-726-361 in 1 PACKAGE01/01/2008
530 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6NDC:50580-726-501 in 1 PACKAGE01/26/2010
650 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7NDC:50580-726-512 in 1 PACKAGE01/26/201011/30/2022
750 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
8NDC:50580-726-381 in 1 PACKAGE01/01/200812/31/2022
845 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
9NDC:50580-726-701 in 1 PACKAGE01/01/200812/31/2022
970 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
10NDC:50580-726-902 in 1 PACKAGE01/26/2010
1045 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
11NDC:50580-726-6675 in 1 PACKAGE, COMBINATION; Type 0: Not a Combination Product01/01/2008
12NDC:50580-726-401 in 1 PACKAGE01/20/2014
1240 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
13NDC:50580-726-912500 in 1 CARTON07/27/2018
131 in 1 POUCH; Type 0: Not a Combination Product
14NDC:50580-726-9250 in 1 TRAY07/12/2018
141 in 1 POUCH; Type 0: Not a Combination Product
15NDC:50580-726-933 in 1 CARTON07/27/2018
151 in 1 POUCH; Type 0: Not a Combination Product
16NDC:50580-726-941 in 1 PACKAGE06/15/2020
1660 in 1 BOTTLE; Type 0: Not a Combination Product
17NDC:50580-726-951 in 1 PACKAGE06/15/2020
1790 in 1 BOTTLE; Type 0: Not a Combination Product
18NDC:50580-726-965 in 1 CARTON05/30/2020
181 in 1 POUCH; Type 0: Not a Combination Product
19NDC:50580-726-9714 in 1 CARTON05/30/2020
191 in 1 POUCH; Type 0: Not a Combination Product
20NDC:50580-726-052500 in 1 CASE03/01/2023
201 in 1 POUCH; Type 0: Not a Combination Product
21NDC:50580-726-2550 in 1 CARTON03/01/2023
211 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA01983501/01/2008
Labeler - Johnson & Johnson Consumer Inc. (878046358)

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