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ANTHELIOS LOTION CORPS ULTRA-FLUIDE - Health Canada Drug Approval Details
Approvals
/
Health Canada
/
ANTHELIOS LOTION CORPS ULTRA-FLUIDE
Authorized
STANDARD
ANTHELIOS LOTION CORPS ULTRA-FLUIDE
laboratoires la roche-posay canada
🇨🇦 Health Canada
Approval Date
Jul 4, 2025
Approval ID
42d5fe64a22602a2
Company
laboratoires la roche-posay canada
Type
Standard
Approval Details
Approval Id
42d5fe64a22602a2
Drug Approval Canada Name
ANTHELIOS LOTION CORPS ULTRA-FLUIDE
Product Name
ANTHELIOS LOTION CORPS ULTRA-FLUIDE
Status
Cancelled Post Market
Status Date
2019-04-01
Original Market Date
2017-10-24
Din
02459515
Drug Class
Human
Dosage Form
Cream
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
0652878001
Company Name
laboratoires la roche-posay canada
Company Address
4895 Hickmore, Montreal, Quebec, Canada, H4T 1K5
Active Ingredients
OCTISALATE
5 % / W/W
AVOBENZONE
3 % / W/W
HOMOSALATE
10 % / W/W
TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID
2 % / W/W
OCTOCRYLENE
5 % / W/W
OXYBENZONE
6 % / W/W
Authorized
Quick Info
Agency
Health Canada
Country
🇨🇦
Approval Date
Jul 4, 2025
Approval ID
42d5fe64a22602a2
Type
Standard
Back to Health Canada Approvals