NDC product
DB Foot Pain Relieving
NDC 43689-0070 · The Magni Company
Key facts
| Product NDC | 43689-0070 |
|---|---|
| Proprietary name | DB Foot Pain Relieving |
| Nonproprietary name | Apis Mellifica, Gelsemium Sempervirens, Gnaphalium |
| Substances | PSEUDOGNAPHALIUM LUTEOALBUM LEAF, GELSEMIUM SEMPERVIRENS WHOLE, APIS MELLIFERA |
| Dosage form | SPRAY |
| Route | TOPICAL |
| Labeler | The Magni Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] |
| Marketing start | Dec 1, 2025 |
| Listing certified through | Dec 31, 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 · Source date: