NDC Code | 50114-6141-2 |
Package Description | 100 TABLET in 1 BOTTLE (50114-6141-2) |
Product NDC | 50114-6141 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Coenzyme Compositum |
Non-Proprietary Name | Beta Vulgaris And Ascorbic Acid And Cysteine And Magnesium Orotate And Manganese Phosphate, Dibasic And Sodium Diethyl Oxalacetate And Niacinamide And Pulsatilla Vulgaris And Pyridoxine Hydrochloride And Riboflavin And Thiamine Hydrochloride And .alpha.-lipoic Acid And .alpha.-ketoglutaric Acid And Cerous Oxalate Nonahydrate And Aconitic Acid, (z)- And Anhydrous Citric Acid And Coenzyme A And Fumaric Acid And Malic Acid And Nadide And Sodium Pyruvate And Succinic Acid |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20030831 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Manufacturer | Heel Inc |
Substance Name | BETA VULGARIS; ASCORBIC ACID; CYSTEINE; MAGNESIUM OROTATE; MANGANESE PHOSPHATE, DIBASIC; SODIUM DIETHYL OXALACETATE; NIACINAMIDE; PULSATILLA VULGARIS; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; .ALPHA.-LIPOIC ACID; .ALPHA.-KETOGLUTARIC ACID; CEROUS OXALATE NONAHYDRATE; ACONITIC ACID, (Z)-; ANHYDROUS CITRIC ACID; COENZYME A; FUMARIC ACID; MALIC ACID; NADIDE; SODIUM PYRUVATE; SUCCINIC ACID; ADENOSINE TRIPHOSPHATE; BARIUM OXALOSUCCINATE; CALCIUM SULFIDE; SULFUR |
Strength | 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |