ANTHELIOS ULTRA-FLUID LOTION
ANTHELIOS ULTRA-FLUID LOTION
Discontinued
DIN Number
02364700
Drug Class
Human
Market Date
Apr 13, 2011
Company
HC
laboratoires la roche-posay canada
Product Information
Detailed information about this Health Canada approved drug product, including dosage form, route of administration, and regulatory classification.
Product Details
Health Canada regulatory and product classification information
Regulatory Identifiers
DIN Number02364700
AIG Number0652878001
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
D02BA30 COMBINATIONS OF PROTECTIVES AGAINST UV-RADIATION
Product Specifications
Dosage FormLotion
Route of AdministrationTopical
AHFS Classification84:80.00
Health Canada Classification
ACTIVE INGREDIENTS (6)
AVOBENZONEActive
Strength: 3.00 % / W/W
Monograph: AVOBENZONE
HOMOSALATEActive
Strength: 10.00 % / W/W
Monograph: HOMOSALATE
OCTISALATEActive
Strength: 5.00 % / W/W
Monograph: OCTISALATE
OCTOCRYLENEActive
Strength: 5.00 % / W/W
Monograph: OCTOCRYLENE
OXYBENZONEActive
Strength: 6.00 % / W/W
Monograph: OXYBENZONE
TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACIDActive
Strength: 2.00 % / W/W
Monograph: TEREPHTHALYLIDENE DICAMPHOR SULFONIC ACID