- Product NDC
- 65121-301
- 11-digit product format
- 651210301
- Labeler code
- 65121
- Product ID
- 65121-301_617b4611-d480-c225-e053-2991aa0aaea1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vitamin C, Vitamin D, Vitamin E, Thiamine, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Biotin, Pantothenic Acid, Chromium
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- Pure Source, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-08-11
- Marketing end
- 0000-00-00
- Substance
- ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXAL PHOSPHATE ANHYDROUS; FOLIC ACID; METHYLCOBALAMIN; BIOTIN; CALCIUM PANTOTHENATE; CHROMIUM PICOLINATE; THIOCTIC ACID; UBIDECARENONE
- Active strength
- 120 mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1
- Pharmacologic classes
- Vitamin C [EPC],Ascorbic Acid [CS],Vitamin D [CS],Vitamin D [EPC],Nicotinic Acid [EPC],Nicotinic Acids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record