Poultice Powder 17.3 mg Powder is a Health Canada–registered veterinary drug (DIN 02025027) held by Austin, Division Of Vétoquinol N.-A. Inc., containing Aluminum Potassium Sulfate. Health Canada lists its status as Cancelled Post Market (status date 27 Jul 2000). Nexara Health has matched 43 registrations of Aluminum Potassium Sulfate across 2 other regulated markets.
Health Canada registration
| DIN | 02025027 |
|---|---|
| Brand name | Poultice Powder |
| Active ingredient | Aluminum Potassium Sulfate |
| Strength | 17.3 mg |
| Dosage form | Powder |
| Route | Topical |
| Company | Austin, Division Of Vétoquinol N.-A. Inc. |
| Status | Cancelled Post Market — 27 Jul 2000 |
| Class | Veterinary |
| ATC | |
| AHFS | |
| Regulator record | Health Canada DPD entry · Product monograph |
Aluminum Potassium Sulfate registered in other markets
43 registrations of the same molecule in 2 national registries outside Canada (first 16 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 |
|---|---|---|---|---|---|---|
| Taiwan | "HCT" Golden GI Plus Suspension 130mg/gm | 回春堂製藥廠股份有限公司 | 懸液劑 | Registered | TFDA | |
| Taiwan | Aluminium Phosphate Paste | Elementis Pharma GmbH | 原料藥糊劑 | Registered | TFDA | |
| Taiwan | Aluminium Phosphate Powder | Elementis Pharma GmbH | （粉） | Registered | TFDA | |
| Taiwan | Aluphate Gel 130mg/Gm (Aluminum Phosphate) "Royal" | 皇佳化學製藥股份有限公司 | 內服凝膠劑 | Registered | TFDA | |
| Taiwan | Aluphosgel (Aluminum Phosphate) "Kingdom" | 中國化學製藥股份有限公司新豐工廠 | 懸液劑 | 已註銷 | TFDA | |
| Taiwan | Aluphosgel Tablets (Aluminum Phosphote) | 景德製藥股份有限公司土城工廠 | 錠劑 | 已註銷 | TFDA | |
| Taiwan | Curer Suspension "Grape King" | 葡萄王企業股份有限公司藥品製造廠 | 懸液劑 | 已註銷 | TFDA | |
| Taiwan | Dried Aluminum Phosphate Gel "Kingdom" | 景德製藥股份有限公司土城工廠 | （粉） | 已註銷 | TFDA | |
| United States | Aluminum Phosphate | SPI Pharma Inc. | Gel | FDA NDC | ||
| United States | Aluminum Phosphate | Elementis Pharma Gmbh | Powder | FDA NDC | ||
| United States | Aluminum sulfate | Holland Company, Inc. | Powder | FDA NDC | ||
| United States | Aluminum Sulfate | Spectrum Laboratory Products, Inc. | Powder | FDA NDC | ||
| United States | Certain Dri Antiperspirant Foot-Lotion | Clarion Brands, LLC | Lotion | listed | FDA NDC | |
| United States | Certain Dri Antiperspirant Hand-Lotion | Clarion Brands, LLC | Lotion | listed | FDA NDC | |
| United States | Certain Dri Clinical Strength Roll On | Clarion Brands, LLC | For Solution | listed | FDA NDC | |
| United States | Certain Dri Roll-On | Clarion Brands, LLC | Liquid | listed | FDA NDC |
See every manufacturer of Aluminum Potassium Sulfate 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 Poultice Powder (DIN 02025027) marketed in Canada?
No. Health Canada lists DIN 02025027 as Cancelled Post Market as of 27 Jul 2000.
Who holds the Canadian licence for this product?
Austin, Division Of Vétoquinol N.-A. Inc. is the company of record in the Health Canada Drug Product Database.
Is Aluminum Potassium Sulfate registered outside Canada?
Yes — Nexara Health has matched 43 registrations in 2 other markets (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 02025027, status date 2000-07-27; national medicine registries: FDA NDC, TFDA. 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 02025027, status date 2000-07-27; national medicine registries: FDA NDC, TFDA.
Health Canada Drug Product Database (DPD), DIN 02025027, status date 2000-07-27; national medicine registries: FDA NDC, TFDA. Last reviewed 2026-09-16. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.