ZYRTEC

This brand name is authorized in Austria, Brazil, Cyprus, Germany, Ecuador, Estonia, Spain, France, Hong Kong, Japan, Lithuania, Malta, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, Turkey, South Africa

Active ingredients

The drug ZYRTEC contains one active pharmaceutical ingredient (API):

1	Cetirizine UNII 64O047KTOA - CETIRIZINE HYDROCHLORIDE
	Cetirizine, a human metabolite of hydroxyzine, is a potent and selective antagonist of peripheral H1-receptors. In vitro receptor binding studies have shown no measurable affinity for other than Η1-receptors.
	Read more about Cetirizine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
ZYRTEC Film-coated tablet / Oral drops / Oral solution	MPI, Generic	Health Sciences Authority (SG)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
R06AE07	Cetirizine	R Respiratory system → R06 Antihistamines for systemic use → R06A Antihistamines for systemic use → R06AE Piperazine derivatives
Discover more medicines within R06AE07

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
BR	Câmara de Regulação do Mercado de Medicamentos	510609601112312, 510609603131314
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	00243748, 00257940, 01433215, 01433221, 01433238, 01467852, 03738203, 04394326, 04394332, 04811126, 04811149, 04811155, 04967029, 04967041, 07736394
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	30024-11-11, 30047-11-11, 30058-12-11
EE	Ravimiamet	1022858, 1022869, 1026526, 1077825, 1077836, 1077847, 1525014, 1525025, 1525047, 1525058, 1525115, 1525126, 1525171, 1525182, 1525193, 1525205, 1525216, 1525227, 1525238, 1525249, 1525250, 1525261, 1525272, 1525283, 1728637, 1731563, 1731574, 1731585, 1826580, 1828537, 1829897, 1829909
ES	Centro de información online de medicamentos de la AEMPS	58481, 60279, 60280, R-1846, R-1846IP, R1846
FR	Base de données publique des médicaments	64949486, 65016707
HK	Department of Health Drug Office	33733, 40728
JP	医薬品医療機器総合機構	4490020F1020, 4490020F2027, 4490020R1027
LT	Valstybinė vaistų kontrolės tarnyba	1003218, 1003219, 1010903, 1010904, 1065605, 1066078, 1069324, 1082128, 1084154, 1085498, 1085687, 1086334, 1088373, 1091412, 1091413
MT	Medicines Authority	MA030/00901, MA030/00902, PI908/01901A
NL	Z-Index G-Standaard, PRK	26298, 38601
NZ	Medicines and Medical Devices Safety Authority	6329, 6330
PL	Rejestru Produktów Leczniczych	100001901, 100074834, 100074857, 100131970, 100412515, 100454164
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W59369001, W59369002, W59369003
SG	Health Sciences Authority	03022P, 08945P, 10796P, 14890P, 15437P
TN	Direction de la Pharmacie et du Médicament	9073241
TR	İlaç ve Tıbbi Cihaz Kurumu	8699624090041, 8699624570048, 8699624590015
ZA	Health Products Regulatory Authority	28/5.7.1/0477, W/5.7.1/148