NDC product
Gynetox
NDC 43857-0565 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0565 |
|---|---|
| Proprietary name | Gynetox |
| Nonproprietary name | Angelica Archangelica, Cimicifuga Racemosa, Zincum Gluconicum, Funiculus Umbilicalis Suis, Lymph Node (Suis), Oophorinum (Suis), Uterus (Suis), Glandula Suprarenalis Suis, Thyroidinum Suis, Boricum Acidum, Kreosotum, Mercurius Solubilis and 8 more |
| Substances | ANGELICA ARCHANGELICA ROOT, BLACK COHOSH, ZINC GLUCONATE, SUS SCROFA UMBILICAL CORD, SUS SCROFA LYMPH, SUS SCROFA OVARY, SUS SCROFA UTERUS, SUS SCROFA ADRENAL GLAND, THYROID, BORIC ACID, WOOD CREOSOTE, MERCURIUS SOLUBILIS and 9 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Fungal Proteins [CS], Increased Histamine Release [PE] and 2 more |
| Marketing start | Feb 18, 2021 |
| 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: