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Bio - Oligo Iodine 12 X Liquid is a Health Canada–registered human drug (DIN 02233558) held by Bio Active Canada Ltd., containing Ferrous Iodide. Health Canada lists its status as Cancelled Post Market (status date 28 Sep 2007). Nexara Health has matched 1 registration of Ferrous Iodide across 1 other regulated market.

Health Canada registration

DIN02233558
Brand nameBio - Oligo Iodine
Active ingredientFerrous Iodide
Strength12 X
Dosage formLiquid
RouteOral
CompanyBio Active Canada Ltd.
StatusCancelled Post Market — 28 Sep 2007
ClassHuman
ATC
AHFS92:02.00* ; See footnote
Regulator recordHealth Canada DPD entry · Product monograph

Ferrous Iodide registered in other markets

1 registration of the same molecule in 1 national registry outside Canada. Each row is taken from the regulator's own published list; status is shown as the registry reports it.

CountryProductMarketing authorisation holderStrengthFormStatusRegistry
United StatesFerrum iodatumBoironPelletlistedFDA NDC

See every manufacturer of Ferrous Iodide 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 Bio - Oligo Iodine (DIN 02233558) marketed in Canada?

No. Health Canada lists DIN 02233558 as Cancelled Post Market as of 28 Sep 2007.

Who holds the Canadian licence for this product?

Bio Active Canada Ltd. is the company of record in the Health Canada Drug Product Database.

Is Ferrous Iodide registered outside Canada?

Yes — Nexara Health has matched 1 registration in 1 other market (see the table above).

Where does this data come from?

Health Canada Drug Product Database (DPD), DIN 02233558, status date 2007-09-28; national medicine registries: 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 02233558, status date 2007-09-28; national medicine registries: FDA NDC.

Health Canada Drug Product Database (DPD), DIN 02233558, status date 2007-09-28; national medicine registries: 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.