Progenite is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Deseret Biologicals. The primary component is Ammonium Carbonate; Barium Chloride Dihydrate; Sodium Borate; Caulophyllum Thalictroides Root; Sodium Carbonate; Saw Palmetto; Juniperus Sabina Leafy Twig; Sulfuric Acid; Allylthiourea; Estrone; Sus Scrofa Fallopian Tube; Sus Scrofa Uterus; Sus Scrofa Hypothalamus; Thyroid, Porcine; Chaste Tree; Conium Maculatum Flowering Top; Graphite; Hyoscyamus Niger; Sepia Officinalis Juice; Selenium; Alcohol, X-ray Exposed (1000 Rad).
| Product ID | 43742-1170_d6e36151-f7bb-4755-8f25-e9519e1170e7 |
| NDC | 43742-1170 |
| Product Type | Human Otc Drug |
| Proprietary Name | Progenite |
| Generic Name | Ammonium Carbonicum, Baryta Muriatica, Borax, Caulophyllum Thalictroides, Natrum Carbonicum, Sabal Serrulata, Sabina, Sulphuricum Acidum, Thiosinaminum, Folliculinum, Tuba Uterina Suis, Uterus Suis, Hypothalamus (suis), Thyroidinum (suis), Agnus Castus, Conium Maculatum, Graphites, Hyoscyamus Niger, Sepia, Selenium Metallicum, X-ray |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-02-19 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Deseret Biologicals |
| Substance Name | AMMONIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; SODIUM BORATE; CAULOPHYLLUM THALICTROIDES ROOT; SODIUM CARBONATE; SAW PALMETTO; JUNIPERUS SABINA LEAFY TWIG; SULFURIC ACID; ALLYLTHIOUREA; ESTRONE; SUS SCROFA FALLOPIAN TUBE; SUS SCROFA UTERUS; SUS SCROFA HYPOTHALAMUS; THYROID, PORCINE; CHASTE TREE; CONIUM MACULATUM FLOWERING TOP; GRAPHITE; HYOSCYAMUS NIGER; SEPIA OFFICINALIS JUICE; SELENIUM; ALCOHOL, X-RAY EXPOSED (1000 RAD) |
| Active Ingredient Strength | 6 [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 | 2018-02-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-02-19 |
| Ingredient | Strength |
|---|---|
| AMMONIUM CARBONATE | 6 [hp_X]/mL |
| SPL SET ID: | 6051c9d5-36ef-4bfa-baab-9862c94805fb |
| Manufacturer | |
| UNII |