TRUE TEST PATCH

Country: Canada

Language: English

Source: Health Canada

Active ingredient:

NICKEL SULFATE; WOOL ALCOHOLS; NEOMYCIN SULFATE; POTASSIUM DICHROMATE; BENZOCAINE; DIBUCAINE HYDROCHLORIDE; TETRACAINE HYDROCHLORIDE; AMYL CINNAMAL; ISOEUGENOL; CINNAMALDEHYDE; EUGENOL; CINNAMYL ALCOHOL; HYDROXYCITRONELLAL; GERANIOL; OAK MOSS; ROSIN; EPOXY RESIN; CLIOQUINOL; CHLOROQUINALDOL; PERUVIAN BALSAM; ETHYLENEDIAMINE DIHYDROCHLORIDE; COBALTOUS CHLORIDE; P-TERT-BUTYLPHENOL FORMALDEHYDE RESIN; METHYLPARABEN; ETHYL PARABEN; PROPYLPARABEN; BUTYLPARABEN; BENZYL PARABEN; DIPHENYLGUANIDINE; ZINC DIBUTYLDITHIOCARBAMATE; N-CYCLOHEXYL-N'-PHENYL-PARA-PHENYLENEDIAMINE; METHYLCHLOROISOTHIAZOLINONE; QUATERNIUM-15; MERCAPTOBENZOTHIAZOLE; P-PHENYLENEDIAMINE; (MORPHOLINOTHIO)BENZOTHIAZOLE; DITHIOBIS (BENZOTHIAZOLE); THIMEROSAL; THIRAM; BIS(1-PIPERIDYLTHIOCARBONYL)DISULFIDE; ZINC DIETHYLDITHIOCARBAMATE; N-ISOPROPYL-N'-PHENYL-PARA-PHENYLENEDIAMINE; N,N'-DIPHENYL-PARA-PHENYLENEDIAMINE; TETRAMETHYLTHIURAM MONOSULFIDE; DISULFIRAM; N-CYCLOHEXYL-2-BENZOTHIAZOLESULFENAMIDE; N-HYDROXYMETHYLSUCCINIMIDE

Available from:

MEKOS LABORATORIES APS

ATC code:

V04CL

INN (International Name):

TESTS FOR ALLERGIC DISEASES

Dosage:

0.16MG; 0.81MG; 0.19MG; 0.019MG; 0.364MG; 0.073MG; 0.073MG; 0.015MG; 0.015MG; 0.034MG; 0.034MG; 0.054MG; 0.054MG; 0.07MG; 0.07MG; 0.69MG; 0.041MG; 0.08MG; 0.08MG; 0.65MG; 0.041MG; 0.016MG; 0.041MG; 0.16MG; 0.16MG; 0.16MG; 0.16MG; 0.16MG; 0.068MG; 0.068MG; 0.025MG; 0.0032MG; 0.081MG; 0.061MG; 0.073MG; 0.02MG; 0.02MG; 0.0065MG; 0.005MG; 0.005MG; 0.068MG; 0.01MG; 0.025MG; 0.005MG; 0.005MG; 0.02MG; 0.15MG

Pharmaceutical form:

PATCH

Composition:

NICKEL SULFATE 0.16MG; WOOL ALCOHOLS 0.81MG; NEOMYCIN SULFATE 0.19MG; POTASSIUM DICHROMATE 0.019MG; BENZOCAINE 0.364MG; DIBUCAINE HYDROCHLORIDE 0.073MG; TETRACAINE HYDROCHLORIDE 0.073MG; AMYL CINNAMAL 0.015MG; ISOEUGENOL 0.015MG; CINNAMALDEHYDE 0.034MG; EUGENOL 0.034MG; CINNAMYL ALCOHOL 0.054MG; HYDROXYCITRONELLAL 0.054MG; GERANIOL 0.07MG; OAK MOSS 0.07MG; ROSIN 0.69MG; EPOXY RESIN 0.041MG; CLIOQUINOL 0.08MG; CHLOROQUINALDOL 0.08MG; PERUVIAN BALSAM 0.65MG; ETHYLENEDIAMINE DIHYDROCHLORIDE 0.041MG; COBALTOUS CHLORIDE 0.016MG; P-TERT-BUTYLPHENOL FORMALDEHYDE RESIN 0.041MG; METHYLPARABEN 0.16MG; ETHYL PARABEN 0.16MG; PROPYLPARABEN 0.16MG; BUTYLPARABEN 0.16MG; BENZYL PARABEN 0.16MG; DIPHENYLGUANIDINE 0.068MG; ZINC DIBUTYLDITHIOCARBAMATE 0.068MG; N-CYCLOHEXYL-N'-PHENYL-PARA-PHENYLENEDIAMINE 0.025MG; METHYLCHLOROISOTHIAZOLINONE 0.0032MG; QUATERNIUM-15 0.081MG; MERCAPTOBENZOTHIAZOLE 0.061MG; P-PHENYLENEDIAMINE 0.073MG; (MORPHOLINOTHIO)BENZOTHIAZOLE 0.02MG; DITHIOBIS (BENZOTHIAZOLE) 0.02MG; THIMEROSAL 0.0065MG; THIRAM 0.005MG; BIS(1-PIPERIDYLTHIOCARBONYL)DISULFIDE 0.005MG; ZINC DIETHYLDITHIOCARBAMATE 0.068MG; N-ISOPROPYL-N'-PHENYL-PARA-PHENYLENEDIAMINE 0.01MG; N,N'-DIPHENYL-PARA-PHENYLENEDIAMINE 0.025MG; TETRAMETHYLTHIURAM MONOSULFIDE 0.005MG; DISULFIRAM 0.005MG; N-CYCLOHEXYL-2-BENZOTHIAZOLESULFENAMIDE 0.02MG; N-HYDROXYMETHYLSUCCINIMIDE 0.15MG

Administration route:

TOPICAL

Units in package:

10

Prescription type:

Schedule D

Therapeutic area:

ALLERGENIC EXTRACTS

Product summary:

Active ingredient group (AIG) number: 4751542001; AHFS:

Authorization status:

CANCELLED POST MARKET

Authorization date:

2013-01-10