| NDC Code | 43742-1954-1 |
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| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-1954-1) |
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| Product NDC | 43742-1954 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Bio Placenta Phase |
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| Non-Proprietary Name | Aesculus Hippocastanum, Sarcolacticum Acidum, Cuprum Sulphuricum, Melilotus Officinalis, Placenta Totalis Suis, Solanum Nigrum, Strophanthus Hispidus, Dhea (dehydroepiandrosterone), Quercetin, Rutin, Natrum Pyruvicum, Secale Cornutum, Vena Suis, Arteria Suis, Funiculus Umbilicalis Suis, Tabacum, Baryta Carbonica, Vipera Berus, Plumbum Iodatum, Astragalus Exscapus, Proteus (vulgaris) |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20210503 |
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| End Marketing Date | 20290422 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | Deseret Biologicals, Inc. |
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| Substance Name | ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING; BARIUM CARBONATE; CLAVICEPS PURPUREA SCLEROTIUM; CUPRIC SULFATE; HORSE CHESTNUT; LACTIC ACID, L-; LEAD IODIDE; MELILOTUS OFFICINALIS TOP; PRASTERONE; PROTEUS VULGARIS; QUERCETIN; RUTIN; SODIUM PYRUVATE; SOLANUM NIGRUM WHOLE; STROPHANTHUS HISPIDUS SEED; SUS SCROFA ARTERY; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; TOBACCO LEAF; VIPERA BERUS VENOM |
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| Strength | 6; 13; 8; 6; 4; 4; 18; 6; 6; 30; 6; 6; 8; 6; 6; 10; 6; 10; 8; 10; 14 |
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| Strength Unit | [hp_C]/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_C]/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 |
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| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] |
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