NDC product
LD Force HP
NDC 43857-0618 · BioActive Nutritional, Inc.
Key facts
| Product NDC | 43857-0618 |
|---|---|
| Proprietary name | LD Force HP |
| Nonproprietary name | Arsenicum Album, Borrelia Burgdorferi Nosode, Chelidonium Majus, Coccus Cacti, Echinacea (Angustifolia), Hydrastis Canadensis, Lycopodium Clavatum, Nasturtium Aquaticum, Phosphorus, Rhus Tox, Taraxacum Officinale, Thymus (Suis) and 3 more |
| Substances | ARSENIC TRIOXIDE, BORRELIA BURGDORFERI, CHELIDONIUM MAJUS WHOLE, PROTORTONIA CACTI, ECHINACEA ANGUSTIFOLIA WHOLE, GOLDENSEAL, LYCOPODIUM CLAVATUM SPORE, NASTURTIUM OFFICINALE, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, TARAXACUM OFFICINALE, SUS SCROFA THYMUS and 3 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | BioActive Nutritional, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Nov 8, 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: