| 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 | HORSE CHESTNUT; LACTIC ACID, L-; CUPRIC SULFATE; MELILOTUS OFFICINALIS TOP; SUS SCROFA PLACENTA; SOLANUM NIGRUM WHOLE; STROPHANTHUS HISPIDUS SEED; PRASTERONE; QUERCETIN; RUTIN; SODIUM PYRUVATE; CLAVICEPS PURPUREA SCLEROTIUM; SUS SCROFA VEIN; SUS SCROFA ARTERY; SUS SCROFA UMBILICAL CORD; TOBACCO LEAF; BARIUM CARBONATE; VIPERA BERUS VENOM; LEAD IODIDE; ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING; PROTEUS VULGARIS |
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| Strength | 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 10; 10; 10; 13; 14; 18; 6; 30 |
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| Strength Unit | [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_C]/mL; [hp_C]/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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