MedPath

SUNSCREEN LOTION SPF 39

SUNSCREEN LOTION SPF 39

Discontinued
DIN Number

02094495

Drug Class

Human

Market Date

Dec 31, 1994

Company
HC

norwood packaging ltd

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 Number02094495
AIG Number0419998033
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 (4)

OCTINOXATEActive
Strength: 8.5 %
Monograph: OCTINOXATE
OCTISALATEActive
Strength: 6 %
Monograph: OCTISALATE
OXYBENZONEActive
Strength: 6 %
Monograph: OXYBENZONE
TITANIUM DIOXIDEActive
Strength: 4 %
Monograph: TITANIUM DIOXIDE

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.