NDC product
LD Force
NDC 43857-1624 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-1624 |
|---|---|
| Proprietary name | LD Force |
| Nonproprietary name | Chelidonium Majus, Echinacea (Angustifolia), Nasturtium Aquaticum, Taraxacum Officinale, Trifolium Pratense, Urtica Dioica, Hydrastis Canadensis, Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Coccus Cacti, Lycopodium Clavatum and 4 more |
| Substances | CHELIDONIUM MAJUS WHOLE, ECHINACEA ANGUSTIFOLIA WHOLE, NASTURTIUM OFFICINALE, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE FLOWER, URTICA DIOICA WHOLE, GOLDENSEAL, SUS SCROFA THYMUS, THYROID, ARSENIC TRIOXIDE, PROTORTONIA CACTI, LYCOPODIUM CLAVATUM SPORE and 4 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Apr 7, 2022 |
| Marketing end | May 6, 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