- Product NDC
- 0642-0204
- 11-digit product format
- 006420204
- Labeler code
- 0642
- Product ID
- 0642-0204_13d4ddf2-f701-441b-87d6-010bc26f677d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vitamin A, Ascorbic Acid, Vitamin D, .Alpha.-Tocopherol, Thiamine Mononitrate, Riboflavin, Niacin, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Biotin, Pantothenic Acid, Magnesium, Zinc, Selenium, Copper, Chromium, Molybdenum, and Iron
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Everett Laboratories, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1996-10-01
- Marketing end
- 0000-00-00
- Substance
- VITAMIN A; ASCORBIC ACID; VITAMIN D; .ALPHA.-TOCOPHEROL; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; PANTOTHENIC ACID; MAGNESIUM; ZINC; SELENIUM; COPPER; CHROMIUM; MOLYBDENUM; IRON
- Active strength
- 4000 [iU]/1; mg/1; [iU]/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; mg/1
- Pharmacologic classes
- Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE],Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record