NDC product
Fibromyalgia Support
NDC 43689-0058 · The Magni Company
Key facts
| Product NDC | 43689-0058 |
|---|---|
| Proprietary name | Fibromyalgia Support |
| Nonproprietary name | Aconitum Napellus, Arsenicum Album, Belladonna, Coniinum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Bichromicum, Lacticum Acidum, Phosphoricum Acidum, Rhus Tox, Uricum Acidum |
| Substances | ACONITUM NAPELLUS WHOLE, ARSENIC TRIOXIDE, ATROPA BELLADONNA, CONIINE, GELSEMIUM SEMPERVIRENS ROOT, HYPERICUM PERFORATUM WHOLE, POTASSIUM DICHROMATE, LACTIC ACID, DL-, PHOSPHORIC ACID, TOXICODENDRON PUBESCENS LEAF, URIC ACID |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | The Magni Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Jan 25, 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: