NDC product
Balanceforce V
NDC 43857-0592 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0592 |
|---|---|
| Proprietary name | Balanceforce V |
| Nonproprietary name | Leonurus Cardiaca, Agaricus Muscarius, Arsenicum Album, Cocculus Indicus, Conium Maculatum, Petroleum, Phosphorus, Pulsatilla (Vulgaris), Tabacum, Theridion |
| Substances | LEONURUS CARDIACA WHOLE, AMANITA MUSCARIA FRUITING BODY, ARSENIC TRIOXIDE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, KEROSENE, PHOSPHORUS, PULSATILLA VULGARIS WHOLE, TOBACCO LEAF, THERIDION CURASSAVICUM |
| 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], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] |
| Marketing start | Jun 1, 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: