NDC product
Chemtox
NDC 43857-0654 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0654 |
|---|---|
| Proprietary name | Chemtox |
| Nonproprietary name | Triticum Aestivum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Rhamnus Purshiana, Stillingia Sylvatica, Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Glandula Suprarenalis Suis, Hepar Suis and 17 more |
| Substances | TRITICUM AESTIVUM WHOLE, BERBERIS VULGARIS ROOT BARK, GLYCYRRHIZA GLABRA, ARCTIUM LAPPA ROOT, FRANGULA ALNUS BARK, FRANGULA PURSHIANA BARK, STILLINGIA SYLVATICA ROOT, TRIFOLIUM PRATENSE FLOWER, ZANTHOXYLUM AMERICANUM BARK, PHYTOLACCA AMERICANA ROOT, SUS SCROFA ADRENAL GLAND, PORK LIVER and 28 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Ammonium Ion Binding Activity [MoA], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA] and 11 more |
| Marketing start | Jan 7, 2025 |
| 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: