PRESUN ULTRA 15 GEL
PRESUN ULTRA 15 GEL
Discontinued
DIN Number
02238653
Drug Class
Human
Market Date
Feb 25, 1999
Company
HC
westwood-squibb, division of bristol-myers squibb canada inc.
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 Number02238653
AIG Number0423152009
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
D02BA30 COMBINATIONS OF PROTECTIVES AGAINST UV-RADIATION
Product Specifications
Dosage FormGel
Route of AdministrationTopical
AHFS Classification84:80.00
Health Canada Classification
ACTIVE INGREDIENTS (4)
AVOBENZONEActive
Strength: 3 %
Monograph: AVOBENZONE
OCTINOXATEActive
Strength: 5 %
Monograph: OCTINOXATE
OCTISALATEActive
Strength: 5 %
Monograph: OCTISALATE
OXYBENZONEActive
Strength: 6 %
Monograph: OXYBENZONE