Drug · DIN 02241556
ENHANCER
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since January 7, 2010; first marketed March 24, 2000.
- Drug Identification Number (DIN)
- 02241556
- Company (DIN owner)
- Tyco HealthcarePointe-Claire, Quebec, Canada
- Schedule
- Ethical
- Dosage form
- Powder For Solution
- Route
- Oral
- Therapeutic class (ATC)
- Barium sulphate with suspending agents V08BA01
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| BARIUM SULFATE | 82 % |
Recalls and safety alerts that mention it
Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “enhancer”. A notice may cover another product or only some lots: read it to see what it covers.
- FEG Eyelash Enhancer: Unauthorized Product with ingredient on prescription drug list.August 18, 2023 · Drugs · Unauthorized product · Type II