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ULTRA-LIGHT UV LOTION - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
ULTRA-LIGHT UV LOTION
Authorized
STANDARD
ULTRA-LIGHT UV LOTION
vichy canada
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
6eb19eff5f3c368f
Company
vichy canada
Type
Standard
Approval Details
Approval Id
6eb19eff5f3c368f
Drug Approval Canada Name
ULTRA-LIGHT UV LOTION
Product Name
ULTRA-LIGHT UV LOTION
Status
Marketed
Status Date
2022-04-13
Original Market Date
2022-04-13
Din
02515806
Drug Class
Human
Dosage Form
Lotion
Route Of Administration
Topical
Schedule
OTC
Ahfs
84:80.00
Atc Original
D02BA30 COMBINATIONS OF PROTECTIVES AGAINST UV-RADIATION
Atc Name
d 02 ba 30
Aig Number
0662887001
Company Name
vichy canada
Company Address
4895 Hickmore, Montreal, Quebec, Canada, H4T 1K5
Active Ingredients
BEMOTRIZINOL
5 % / W/W
AVOBENZONE
3 % / W/W
DROMETRIZOLE TRISILOXANE
3.5 % / W/W
HOMOSALATE
2 % / W/W
OCTISALATE
5 % / W/W
OCTOCRYLENE
5 % / W/W
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
6eb19eff5f3c368f
Type
Standard
Back to Health Canada Approvals