NDC product
Bio Placenta Phase
NDC 43742-2240 · Deseret Biologicals, Inc.
Key facts
| Product NDC | 43742-2240 |
|---|---|
| Proprietary name | Bio Placenta Phase |
| Nonproprietary 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) and 9 more |
| Substances | 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 and 9 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Deseret Biologicals, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] |
| Marketing start | Nov 19, 2024 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: