DRULA FADE CREAM SUPERFORTE MEDICATED
DRULA FADE CREAM SUPERFORTE MEDICATED
Discontinued
DIN Number
02010593
Drug Class
Human
Market Date
Dec 31, 1994
Company
HC
drula-fabrik, dr. o. druckery gmbh
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 Number02010593
AIG Number0223063004
Classification & Schedule
C
Drug Class
Human
S
Schedule
Prescription
A
ATC Code
D11AX11 HYDROQUINONE
Product Specifications
Dosage FormCream
Route of AdministrationTopical
AHFS Classification84:50.04
Health Canada Classification
ACTIVE INGREDIENTS (2)
HYDROQUINONEActive
Strength: 4 G / 100 G
Monograph: HYDROQUINONE
OXYBENZONEActive
Strength: 4 G / 100 G
Monograph: OXYBENZONE