Details for: 29 ESSENTIAL VITAMINS AND MINERALS (FOR PEOPLE 50+)

Product description

Product name: 29 ESSENTIAL VITAMINS AND MINERALS (FOR PEOPLE 50+)

Company name: VITA HEALTH PRODUCTS INC

DIN: 02231519

Status: Cancelled Post Market

Status date: 2005-07-20

Active ingredient(s)	Strength
ASCORBIC ACID (ASCORBIC ACID)	90 MG
BETA-CAROTENE	3000 UNIT
BIOTIN	45 MCG
CALCIUM (CALCIUM PHOSPHATE (DIBASIC), CALCIUM CARBONATE)	200 MG
CHLORINE (POTASSIUM CHLORIDE)	72 MG
CHROMIUM (CHROMIC CHLORIDE)	100 MCG
COPPER (CUPRIC OXIDE)	2 MG
D-PANTOTHENIC ACID (CALCIUM D-PANTOTHENATE)	10 MG
FOLIC ACID	0.4 MG
IODINE (POTASSIUM IODIDE)	0.15 MG
IRON (FERROUS FUMARATE)	4 MG
MAGNESIUM (MAGNESIUM OXIDE)	100 MG
MANGANESE (MANGANESE SULFATE)	5 MG
MOLYBDENUM (SODIUM MOLYBDATE)	25 MCG
NICKEL (NICKEL SULFATE)	5 MCG
NICOTINAMIDE	40 MG
PHOSPHORUS (CALCIUM PHOSPHATE (DIBASIC))	125 MG
POTASSIUM (POTASSIUM CHLORIDE)	80 MG
SELENIUM (SODIUM SELENATE)	25 MCG
SILICON (SODIUM METASILICATE)	0.01 MG
TIN (STANNOUS CHLORIDE)	0.01 MG
VANADIUM (SODIUM METAVANADATE)	10 MCG
VITAMIN A (VITAMIN A ACETATE)	3000 UNIT
VITAMIN B12 (VITAMIN B12)	25 MCG
VITAMIN B1 (THIAMINE MONONITRATE)	2.25 MG
VITAMIN B2 (VITAMIN B2)	3.2 MG
VITAMIN B6 (PYRIDOXINE HYDROCHLORIDE)	3 MG
VITAMIN D3 (VITAMIN D3)	400 UNIT
VITAMIN E (DL-ALPHA TOCOPHERYL ACETATE)	45 UNIT
ZINC (ZINC OXIDE)	15 MG

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For consumers

Resource	Description
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.

For health care professionals

Resource	Description
Report a serious adverse drug reaction (for hospitals)	Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals.

For researchers

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

All resources

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.
Report a serious adverse drug reaction (for hospitals)	Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals.

Resource	Description
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.
Report a serious adverse drug reaction (for hospitals)	Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals.