| NDC Code | 43742-2240-1 |
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| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-2240-1) |
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| Product NDC | 43742-2240 |
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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, Arteria Suis, Astragalus Exscapus, Baryta Carbonica, Cuprum Sulphuricum, Dhea (dehydroepiandrosterone), Funiculus Umbilicalis Suis, Melilotus Officinalis, Natrum Pyruvicum, Placenta Totalis Suis, Plumbum Iodatum, Proteus (vulgaris), Quercetin, Rutin, Sarcolacticum Acidum, Secale Cornutum, Solanum Nigrum, Strophanthus Hispidus, Tabacum, Vena Suis, Vipera Berus |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20241119 |
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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; SUS SCROFA ARTERY; ASTRAGALUS EXSCAPUS WHOLE FLOWERING/FRUITING; BARIUM CARBONATE; CUPRIC SULFATE; PRASTERONE; SUS SCROFA UMBILICAL CORD; MELILOTUS OFFICINALIS TOP; SODIUM PYRUVATE; SUS SCROFA PLACENTA; LEAD IODIDE; PROTEUS VULGARIS; QUERCETIN; RUTIN; LACTIC ACID, L-; CLAVICEPS PURPUREA SCLEROTIUM; SOLANUM NIGRUM WHOLE; STROPHANTHUS HISPIDUS SEED; TOBACCO LEAF; SUS SCROFA VEIN; 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; 20 |
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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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