NDC product
PMS
NDC 43857-0314 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0314 |
|---|---|
| Proprietary name | PMS |
| Nonproprietary name | Angelica Archangelica, Cimicifuga Racemosa, Fucus Vesiculosus, Hypothalamus Suis, Magnesium Gluconicum Dihydricum, Oophorinum (Suis) Pyridoxinum Hydrochloricum, Bovista, Cuprum Metallicum, Sepia, Zincum Metallicum, Lachesis Mutus |
| Substances | ANGELICA ARCHANGELICA ROOT, BLACK COHOSH, FUCUS VESICULOSUS, SUS SCROFA HYPOTHALAMUS, MAGNESIUM GLUCONATE, SUS SCROFA OVARY, PYRIDOXINE HYDROCHLORIDE, LYCOPERDON UTRIFORME FRUITING BODY, COPPER, SEPIA OFFICINALIS JUICE, ZINC, LACHESIS MUTA VENOM |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Calculi Dissolution Agent [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE] and 10 more |
| Marketing start | Jul 14, 2014 |
| 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: