NDC product
CV TOX
NDC 43857-0637 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0637 |
|---|---|
| Proprietary name | CV TOX |
| Nonproprietary name | Cochlearia Armoracia, Echinacea (Angustifolia), Lomatium Dissectum, Tabebuia Impetiginosa, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Bovine, Thymus (Suis), Aranea Diadema, Ipecacuanha, Lycopodium Clavatum, Muriaticum Acidum and 13 more |
| Substances | HORSERADISH, ECHINACEA ANGUSTIFOLIA WHOLE, LOMATIUM DISSECTUM ROOT, HANDROANTHUS IMPETIGINOSUS BARK, GOLDENSEAL, PROPOLIS WAX, BOS TAURUS ADRENAL GLAND, SUS SCROFA THYMUS, ARANEUS DIADEMATUS, IPECAC, LYCOPODIUM CLAVATUM SPORE, HYDROCHLORIC ACID and 12 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], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC] and 2 more |
| Marketing start | Nov 7, 2023 |
| 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: