Metabopath is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energetix Corp. The primary component is Adenosine Cyclic Phosphate; .alpha.-ketoglutaric Acid; Adenosine Triphosphate Disodium; Berberis Vulgaris Root Bark; Anhydrous Citric Acid; Coenzyme A; Herring Sperm Dna; Fumaric Acid; Glycyrrhiza Glabra; Calcium Sulfide; Arctium Lappa Root; Magnesium Phosphate, Dibasic; Manganese Acetate Tetrahydrate; Nadide; Sodium Chloride; Sodium Diethyl Oxalacetate; Sodium Pyruvate; Niacinamide; Pulsatilla Vulgaris; Pyridoxine Hydrochloride; Frangula Purshiana Bark; Riboflavin; Saccharomyces Cerevisiae Rna; Silicon Dioxide; Succinic Acid; Sulfur; Thiamine Hydrochloride; Thyroid, Bovine; Trifolium Pratense Flower; Zanthoxylum Americanum Bark; Zinc Gluconate.
Product ID | 64578-0102_1ca77586-6562-4101-bce9-913e1c2f6c38 |
NDC | 64578-0102 |
Product Type | Human Otc Drug |
Proprietary Name | Metabopath |
Generic Name | Adenosinum Cyclophosphoricum, Adenosinum Triphosphoricum Dinatrum, Alpha-ketoglutaricum Acidum, Berberis Vulgaris, Citricum Acidum, Coenzyme A, Dna, Fumaricum Acidum, Glycyrrhiza Glabra, Hepar Sulphuris Calcareum, Lappa Major, Magnesia Phosphorica, Manganum Aceticum, Nadidum, Natrum Muriaticum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pulsatilla, Pyridoxinum Hydrochloricum, Rhamnus Purshiana, Riboflavinum, Rna, Silicea, Succinicum Acidum, Sulphur, Thiaminum Hydrochloricum, |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2014-08-08 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Energetix Corp |
Substance Name | ADENOSINE CYCLIC PHOSPHATE; .ALPHA.-KETOGLUTARIC ACID; ADENOSINE TRIPHOSPHATE DISODIUM; BERBERIS VULGARIS ROOT BARK; ANHYDROUS CITRIC ACID; COENZYME A; HERRING SPERM DNA; FUMARIC ACID; GLYCYRRHIZA GLABRA; CALCIUM SULFIDE; ARCTIUM LAPPA ROOT; MAGNESIUM PHOSPHATE, DIBASIC; MANGANESE ACETATE TETRAHYDRATE; NADIDE; SODIUM CHLORIDE; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; NIACINAMIDE; PULSATILLA VULGARIS; PYRIDOXINE HYDROCHLORIDE; FRANGULA PURSHIANA BARK; RIBOFLAVIN; SACCHAROMYCES CEREVISIAE RNA; SILICON DIOXIDE; SUCCINIC ACID; SULFUR; THIAMINE HYDROCHLORIDE; THYROID, BOVINE; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARK; ZINC GLUCONATE |
Active Ingredient Strength | 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2016-05-09 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-05-09 |
Ingredient | Strength |
---|---|
ADENOSINE CYCLIC PHOSPHATE | 8 [hp_X]/mL |