Acidum Citricum-Injeel Liq (D10-D200) 10 D Liquid is a Health Canada–registered human drug (DIN 02037378) held by Biologische Heilmittel Heel GmbH, containing Citric Acid. Health Canada lists its status as Cancelled Post Market (status date 05 Mar 1997). Nexara Health has matched 20 registrations of Citric Acid across 5 other regulated markets.
Health Canada registration
| DIN | 02037378 |
|---|---|
| Brand name | Acidum Citricum-Injeel Liq (D10-D200) |
| Active ingredient | Citric Acid |
| Strength | 10 D |
| Dosage form | Liquid |
| Route | Oral |
| Company | Biologische Heilmittel Heel GmbH |
| Status | Cancelled Post Market — 05 Mar 1997 |
| Class | Human |
| ATC | |
| AHFS | 92:02.00* ; See footnote |
| Regulator record | Health Canada DPD entry · Product monograph |
Citric Acid registered in other markets
20 registrations of the same molecule in 5 national registries outside Canada (first 18 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 |
|---|---|---|---|---|---|---|
| Australia | Citric Acid Monohydrate | — | EP | PBS | ||
| Singapore | Potassium Citrate Mixture BP | Icm Pharma Pte. Ltd. | 228.5mg/5ml&&1.5g/5ml | Solution | General Sale List | HSA |
| Taiwan | Citric Acid Powder | Eli. Lilly & Co. | （粉） | 已註銷 | TFDA | |
| Taiwan | Citric Acid USP | Consolidate Midland Corp. | （粉） | 已註銷 | TFDA | |
| Taiwan | Citric Acid, Anhydrous | Roche Vitamins Ltd. | （粉） | 已註銷 | TFDA | |
| United Kingdom | Citric acid 17.79g / Magnesium carbonate 11.57g effervescent powder sachets sugar free | — | 0001 | NHS dm+d VMP | ||
| United Kingdom | Citric acid 1g/10ml oral solution sachets | — | 0002 | NHS dm+d VMP | ||
| United Kingdom | Citric acid 1g/10ml oral solution unit dose sugar free | — | 0002 | NHS dm+d VMP | ||
| United Kingdom | Citric acid monohydrate 20mg/5ml / Ipecacuanha liquid extract 10microlitres/5ml oral solution sugar free | — | 0001 | NHS dm+d VMP | ||
| United Kingdom | Citric acid monohydrate 334mg/5ml / Potassium citrate monohydrate 550mg/5ml / Sodium citrate dihydrate 500mg/5ml oral solution | — | 0001 | NHS dm+d VMP | ||
| United States | Citric Acid Anhydrous | Fagron Inc | Powder | FDA NDC | ||
| United States | Citric Acid Anhydrous | 60929 | Powder | FDA NDC | ||
| United States | Earthmed Soothe Chewable Cherry | Earthmed LLC | Chewable Gel | listed | FDA NDC | |
| United States | Earthmed Soothe Chewable Orange | Earthmed LLC | Chewable Gel | listed | FDA NDC | |
| United States | Earthmed Soothe Chewable Strawberry | Earthmed LLC | Chewable Gel | listed | FDA NDC | |
| United States | Earthmed Soothe Chewable Watermelon | Earthmed LLC | Chewable Gel | listed | FDA NDC | |
| United States | Soothe Chewable | Carolina Cannabis Creations LLC | Chewable Gel | listed | FDA NDC | |
| United States | Soothe Chewable | Carolina Cannabis Creations LLC | Chewable Gel | listed | FDA NDC |
See every manufacturer of Citric Acid 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 Acidum Citricum-Injeel Liq (D10-D200) (DIN 02037378) marketed in Canada?
No. Health Canada lists DIN 02037378 as Cancelled Post Market as of 05 Mar 1997.
Who holds the Canadian licence for this product?
Biologische Heilmittel Heel GmbH is the company of record in the Health Canada Drug Product Database.
Is Citric Acid registered outside Canada?
Yes — Nexara Health has matched 20 registrations in 5 other markets (see the table above).
Where does this data come from?
Health Canada Drug Product Database (DPD), DIN 02037378, status date 1997-03-05; national medicine registries: FDA NDC, HSA, NHS dm+d VMP, PBS, 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 02037378, status date 1997-03-05; national medicine registries: FDA NDC, HSA, NHS dm+d VMP, PBS, TFDA.
Health Canada Drug Product Database (DPD), DIN 02037378, status date 1997-03-05; national medicine registries: FDA NDC, HSA, NHS dm+d VMP, PBS, 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.