Endocrinpath is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energetix Corp. The primary component is Alfalfa; Borage; Oyster Shell Calcium Carbonate, Crude; Ceanothus Americanus Leaf; Anhydrous Citric Acid; Fucus Vesiculosus; Ginkgo; Sus Scrofa Adrenal Gland; Glycyrrhiza Glabra; Centella Asiatica; Bos Taurus Hypothalamus; Potassium Phosphate, Dibasic; Sus Scrofa Pancreas; Phytolacca Americana Root; Bos Taurus Pituitary Gland; Smilax Ornata Root; Silicon Dioxide; Syzygium Cumini Seed; Taraxacum Officinale; Thyroid, Bovine.
Product ID | 64578-0101_17d36106-9339-4277-9330-36ae3ed6975d |
NDC | 64578-0101 |
Product Type | Human Otc Drug |
Proprietary Name | Endocrinpath |
Generic Name | Alfalfa, Borago Officinalis, Calcarea Carbonica, Ceanothus Americanus, Citricum Acidum, Fucus Vesiculosus, Ginkgo Biloba, Glandula Suprarenalis Suis, Glycyrrhiza Glabra, Hydrocotyle Asiatica, Hypothalamus (bovine), Kali Phosphoricum, Pancreas Suis, Phytolacca Decandra, Pituitarum Posterium (bovine), Sarsaparilla (smilax Regelii), Silicea, Syzygium Jambolanum, Taraxacum Officinale, Thyroidinum (bovine) |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2014-11-20 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Energetix Corp |
Substance Name | ALFALFA; BORAGE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CEANOTHUS AMERICANUS LEAF; ANHYDROUS CITRIC ACID; FUCUS VESICULOSUS; GINKGO; SUS SCROFA ADRENAL GLAND; GLYCYRRHIZA GLABRA; CENTELLA ASIATICA; BOS TAURUS HYPOTHALAMUS; POTASSIUM PHOSPHATE, DIBASIC; SUS SCROFA PANCREAS; PHYTOLACCA AMERICANA ROOT; BOS TAURUS PITUITARY GLAND; SMILAX ORNATA ROOT; SILICON DIOXIDE; SYZYGIUM CUMINI SEED; TARAXACUM OFFICINALE; THYROID, BOVINE |
Active Ingredient Strength | 15 [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 | 2016-03-24 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-03-24 |
Ingredient | Strength |
---|---|
ALFALFA | 15 [hp_X]/mL |
SPL SET ID: | 70f84941-b8a1-48f4-9c05-554e554f0049 |
Manufacturer | |
UNII |