NDC product
Traumex
NDC 62795-2302 · MediNatura Inc
Key facts
| Product NDC | 62795-2302 |
|---|---|
| Proprietary name | Traumex |
| Nonproprietary name | ARNICA MONTANA WHOLE, CALENDULA OFFICINALIS FLOWERING TOP, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, BAPTISIA TINCTORIA ROOT, BELLIS PERENNIS WHOLE, ECHINACEA ANGUSTIFOLIA WHOLE, ACONITUM NAPELLUS WHOLE, MATRICARIA CHAMOMILLA WHOLE, ACHILLEA MILLEFOLIUM WHOLE, ATROPA BELLADONNA, HYPERICUM PERFORATUM WHOLE, RUTA GRAVEOLENS FLOWERING TOP and COMFREY ROOT |
| Substances | ARNICA MONTANA WHOLE, CALENDULA OFFICINALIS FLOWERING TOP, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, BAPTISIA TINCTORIA ROOT, BELLIS PERENNIS WHOLE, ECHINACEA ANGUSTIFOLIA WHOLE, ACONITUM NAPELLUS WHOLE, MATRICARIA CHAMOMILLA WHOLE, ACHILLEA MILLEFOLIUM WHOLE, ATROPA BELLADONNA, HYPERICUM PERFORATUM WHOLE, RUTA GRAVEOLENS FLOWERING TOP and 1 more |
| Dosage form | TABLET, CHEWABLE |
| Route | ORAL |
| Labeler | MediNatura Inc |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Mar 20, 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: