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Unda 245 4 X Drops ; Granules ; Liquid ; Pellet ; Tablet is a Health Canada–registered human drug (DIN 02233243) held by Seroyal International Inc., containing Thuja Occidentalis. Health Canada lists its status as Cancelled Post Market (status date 06 Jul 2009). Nexara Health has matched 32 registrations of Thuja Occidentalis across 3 other regulated markets, 2 of them in the same strength and dosage form.

Health Canada registration

DIN02233243
Brand nameUnda 245
Active ingredientThuja Occidentalis
Strength4 X
Dosage formDrops ; Granules ; Liquid ; Pellet ; Tablet
RouteOral
CompanySeroyal International Inc.
StatusCancelled Post Market — 06 Jul 2009
ClassHuman
ATC
AHFS92:02.00* ; See footnote
Regulator recordHealth Canada DPD entry · Product monograph

Thuja Occidentalis registered in other markets

32 registrations of the same molecule in 3 national registries outside Canada (first 14 shown, exact strength and form first). Each row is taken from the regulator's own published list; status is shown as the registry reports it.

CountryProductMarketing authorisation holderStrengthFormStatusRegistry
United Arab EmiratesThuja - Dr. ReckewegPHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. GMBH, Germany, BENSHEIM1X - 200CTabletActiveEDE
United StatesBestmade Natural Products Thuja OccBestmade Natural ProductsTablet, SolublelistedFDA NDC
NetherlandsThuja occidentalisBOIRON (Messimy)4 DH t/m 60 DH#2 CH t/m 200 CH#6 K t/m 100.000 K#1 LM t/m 30 LMUitsluitend apotheek of drogistEU national register
NetherlandsThuja occidentalisBOIRON (Messimy)4 DH t/m 60 DH#2 CH t/m 200 CH#6 K t/m 100.000 K#1 LM t/m 30 LMGlobuliUitsluitend apotheek of drogistEU national register
United Arab EmiratesThuja - Dr. ReckewegPHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. GMBH, Germany, BENSHEIMMT - 200CDropsActiveEDE
United Arab EmiratesThuja - Dr. ReckewegPHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. GMBH, Germany, BENSHEIMMT - 200CSolutionActiveEDE
United Arab EmiratesThuya Occidentalis - BoironBOIRON, France, MessimyMT to 200 CHPillulesActiveEDE
United StatesBM Thuja OccBM Private LimitedLiquidlistedFDA NDC
United StatesFemmesil Cleansing BarAidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions, LLCSoaplistedFDA NDC
United StatesH-Age Spots FormulaHealing Natural Oils LLCOillistedFDA NDC
United StatesNaturasil Skin TagsNature's Innovation, Inc.LiquidlistedFDA NDC
United StatesNaturasil WartsNature's Innovation, Inc.LiquidlistedFDA NDC
United StatesTerrasil Antifungal Cleansing BarAidance Skincare & Topical Solutions, LLCSoaplistedFDA NDC
United StatesTerrasil Fast and Natural Wart RemovalAidance Skincare & Topical Solutions, LLCOintmentlistedFDA NDC

See every manufacturer of Thuja Occidentalis worldwide →

Sourcing through Nexara Health

Nexara Health is a Health Canada–licensed wholesaler (DEL #3-002896) in Winnipeg. This DIN is not currently marketed in Canada. The registrations above show which regulated markets hold an equivalent presentation that can be sourced for clinical comparator use or on a named-patient basis under Health Canada's Special Access Programme. Request a quote or read how named-patient and foreign-pack supply works in Canada.

Frequently asked questions

Is Unda 245 (DIN 02233243) marketed in Canada?

No. Health Canada lists DIN 02233243 as Cancelled Post Market as of 06 Jul 2009.

Who holds the Canadian licence for this product?

Seroyal International Inc. is the company of record in the Health Canada Drug Product Database.

Is Thuja Occidentalis registered outside Canada?

Yes — Nexara Health has matched 32 registrations in 3 other markets, including 2 in the same strength and dosage form (see the table above).

Where does this data come from?

Health Canada Drug Product Database (DPD), DIN 02233243, status date 2009-07-06; national medicine registries: EDE, EU national register, FDA NDC. Nexara Health re-checks these sources weekly and shows the last verification date at the top of the page.

Source: Health Canada Drug Product Database (DPD), DIN 02233243, status date 2009-07-06; national medicine registries: EDE, EU national register, FDA NDC.

Health Canada Drug Product Database (DPD), DIN 02233243, status date 2009-07-06; national medicine registries: EDE, EU national register, FDA NDC. Last reviewed 2026-09-16. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.