NDC product
Bio Chem Detox
NDC 43857-0613 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0613 |
|---|---|
| Proprietary name | Bio Chem Detox |
| Nonproprietary name | Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Rhamnus Purshiana, Stillingia Sylvatica, Trifolium Pratense, Triticum Aestivum, Xanthoxylum Fraxineum, Phytolacca Decandra, Glandula Suprarenalis Suis, Hepar Suis, Lymph Node (Suis) and 16 more |
| Substances | BERBERIS VULGARIS ROOT BARK, GLYCYRRHIZA GLABRA, ARCTIUM LAPPA ROOT, FRANGULA PURSHIANA BARK, STILLINGIA SYLVATICA ROOT, TRIFOLIUM PRATENSE FLOWER, TRITICUM AESTIVUM WHOLE, ZANTHOXYLUM AMERICANUM BARK, PHYTOLACCA AMERICANA ROOT, SUS SCROFA ADRENAL GLAND, PORK LIVER, SUS SCROFA LYMPH and 19 more |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC] and 3 more |
| Marketing start | Sep 2, 2021 |
| Listing certified through | Dec 31, 2027 |
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: