MAGNESIA USTA-INJEEL FORTE LIQ
MAGNESIA USTA-INJEEL FORTE LIQ
Discontinued
DIN Number
02064618
Drug Class
Human
Market Date
Dec 31, 1994
Company
HC
Biologische Heilmittel Heel 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 Number02064618
AIG Number0101577004
Classification & Schedule
C
Drug Class
Human
S
Schedule
Homeopathic
Product Specifications
Dosage FormLiquid
Route of AdministrationOral
AHFS Classification92:02.00*
Health Canada Classification
ACTIVE INGREDIENTS (1)
MAGNESIUM OXIDEActive
Strength: 6 D / 1.1 ML
Monograph: MAGNESIUM OXIDE