ULTRAPLAST ANALGESIC SPRAY
ULTRAPLAST ANALGESIC SPRAY
Discontinued
DIN Number
00257036
Drug Class
Human
Market Date
Dec 31, 1985
Company
HC
wallace, cameron and company 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 Number00257036
AIG Number0403090001
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
M02AC PREPARATIONS WITH SALICYLIC ACID DERIVATIVES
Product Specifications
Dosage FormAerosol
Route of AdministrationTopical
AHFS Classification28:08.04.24
Health Canada Classification
ACTIVE INGREDIENTS (4)
ETHYL SALICYLATEActive
Strength: 4.8 %
Monograph: ETHYL SALICYLATE
GLYCOL SALICYLATEActive
Strength: 4.8 %
Monograph: GLYCOL SALICYLATE
METHYL NICOTINATEActive
Strength: 1.6 %
Monograph: METHYL NICOTINATE
METHYL SALICYLATEActive
Strength: .96 %
Monograph: METHYL SALICYLATE