NDC product
GUNA-ORAL
NDC 17089-452 · Guna spa
Key facts
| Product NDC | 17089-452 |
|---|---|
| Proprietary name | GUNA-ORAL |
| Nonproprietary name | ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - SUS SCROFA TOOTH… |
| Substances | ACONITUM NAPELLUS, ARNICA MONTANA, ATROPA BELLADONNA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, WITCH HAZEL, CALCIUM SULFIDE, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, COMFREY ROOT, SUS SCROFA TOOTH |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | May 27, 2010 |
| 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: