Drug · DIN 00520128
OPTREX EYE DROPS
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 September 9, 1996; first marketed December 31, 1981.
- Drug Identification Number (DIN)
- 00520128
- Company (DIN owner)
- Optrex Labs Ltd.Basingstoke, Saone Et Loire, United Kingdom
- Schedule
- Non-prescription drugs
- Dosage form
- Liquid
- Route
- Ophthalmic
- Therapeutic class (ATC)
- Sodium borate S01AX07
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| HAMAMELIS VIRGINIANA | 12.5 % | |
| BORIC ACID | 1.08 % | |
| GLYCERINE | 1 % | |
| SODIUM BORATE | .215 % | |
| ALLANTOIN | .08 % |
Other DINs named OPTREX EYE DROPS
- DIN 02185482 · Cancelled Post Market
- DIN 02236576 · Cancelled Post Market