Homeo-Form Ca-Liq 3 X Liquid is a Health Canada–registered human drug (DIN 02140608) held by Homeocan Inc., containing Thuja Occidentalis. Health Canada lists its status as Cancelled Post Market (status date 04 Aug 2009). Nexara Health has matched 32 registrations of Thuja Occidentalis across 3 other regulated markets, 8 of them in the same strength and dosage form.
Health Canada registration
| DIN | 02140608 |
|---|---|
| Brand name | Homeo-Form Ca-Liq |
| Active ingredient | Thuja Occidentalis |
| Strength | 3 X |
| Dosage form | Liquid |
| Route | Oral |
| Company | Homeocan Inc. |
| Status | Cancelled Post Market — 04 Aug 2009 |
| Class | Human |
| ATC | |
| AHFS | 92:02.00* ; See footnote |
| Regulator record | Health 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.
| Country | Product | Marketing authorisation holder | Strength | Form | Status | Registry |
|---|---|---|---|---|---|---|
| United Arab Emirates | Thuja - Dr. Reckeweg | PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. GMBH, Germany, BENSHEIM | MT - 200C | Drops | Active | EDE |
| United States | BM Thuja Occ | BM Private Limited | Liquid | listed | FDA NDC | |
| United States | Naturasil Skin Tags | Nature's Innovation, Inc. | Liquid | listed | FDA NDC | |
| United States | Naturasil Warts | Nature's Innovation, Inc. | Liquid | listed | FDA NDC | |
| United States | Thuja occidentalis | Newton Laboratories, Inc. | Liquid | listed | FDA NDC | |
| United States | Thuja Occidentalis 30C | Natural Creations, Inc | Liquid | listed | FDA NDC | |
| United States | Thuja occidentalis 7140 | Professional Complementary Health Formulas | Liquid | listed | FDA NDC | |
| United States | Walgreens Skin Tag Treatment | Walgreens | Liquid | listed | FDA NDC | |
| Netherlands | Thuja occidentalis | BOIRON (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 LM | Uitsluitend apotheek of drogist | EU national register | |
| Netherlands | Thuja occidentalis | BOIRON (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 LM | Globuli | Uitsluitend apotheek of drogist | EU national register |
| United Arab Emirates | Thuja - Dr. Reckeweg | PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. GMBH, Germany, BENSHEIM | MT - 200C | Solution | Active | EDE |
| United Arab Emirates | Thuja - Dr. Reckeweg | PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. GMBH, Germany, BENSHEIM | 1X - 200C | Tablet | Active | EDE |
| United Arab Emirates | Thuya Occidentalis - Boiron | BOIRON, France, Messimy | MT to 200 CH | Pillules | Active | EDE |
| United States | Bestmade Natural Products Thuja Occ | Bestmade Natural Products | Tablet, Soluble | listed | FDA 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 Homeo-Form Ca-Liq (DIN 02140608) marketed in Canada?
No. Health Canada lists DIN 02140608 as Cancelled Post Market as of 04 Aug 2009.
Who holds the Canadian licence for this product?
Homeocan 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 8 in the same strength and dosage form (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 02140608, status date 2009-08-04; 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 02140608, status date 2009-08-04; national medicine registries: EDE, EU national register, FDA NDC.
Health Canada Drug Product Database (DPD), DIN 02140608, status date 2009-08-04; 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.