TWIN ULTRA LIQUID GRAPE FLAVOR
TWIN ULTRA LIQUID GRAPE FLAVOR
Discontinued
DIN Number
01984225
Drug Class
Human
Market Date
Dec 31, 1995
Company
HC
twin laboratories 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 Number01984225
AIG Number0923745001
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
A11JB VITAMINS WITH MINERALS
Product Specifications
Dosage FormLiquid
Route of AdministrationOral
AHFS Classification88:28.01*
Health Canada Classification
ACTIVE INGREDIENTS (9)
ASCORBIC ACIDActive
Strength: .127 MG / ML
Monograph: ASCORBIC ACID
BIOTINActive
Strength: .634 MCG / ML
Monograph: BIOTIN
CHROMIUMActive
Strength: .4 MCG / ML
Monograph: CHROMIUM
D-PANTOTHENIC ACIDActive
Strength: .211 MG / ML
Monograph: D-PANTOTHENIC ACID
NICOTINAMIDEActive
Strength: .042 MG / ML
Monograph: NICOTINAMIDE
POTASSIUM (POTASSIUM PHOSPHATE DIBASIC)Active
Strength: .209 MG / ML
Monograph: POTASSIUM (POTASSIUM PHOSPHATE DIBASIC)
PYRIDOXINE HYDROCHLORIDEActive
Strength: 4 MCG / ML
Monograph: PYRIDOXINE HYDROCHLORIDE
THIAMINE HYDROCHLORIDEActive
Strength: 3 MCG / ML
Monograph: THIAMINE HYDROCHLORIDE
VITAMIN B2Active
Strength: 4 MCG / ML
Monograph: VITAMIN B2