Drug · DIN 02308606
MULTI-AGE CORRECTION
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 July 29, 2014; first marketed September 1, 2008.
- Drug Identification Number (DIN)
- 02308606
- Company (DIN owner)
- Sanofi Consumer Health IncLaval, Quebec, Canada
- Schedule
- Non-prescription drugs
- Dosage form
- Cream
- Route
- Topical
- Therapeutic class (ATC)
- Combinations of protectives against uv-radiation D02BA30
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| OCTINOXATE | 7.5 % | W/W |
| OXYBENZONE | 5.0 % | W/W |