NDC product
GUNA HEALTHY BRAIN
NDC 17089-500 · Guna spa
Key facts
| Product NDC | 17089-500 |
|---|---|
| Proprietary name | GUNA HEALTHY BRAIN |
| Nonproprietary name | Citrullus colocynthis fruit pulp - ubidecarenone - sus scrifa adrenal gland - sus scrofa placenta - selenium - thuja occidentalis leafy twig - conium maculatum flowering top - sus scrofa embryo… |
| Substances | CITRULLUS COLOCYNTHIS FRUIT PULP, SUS SCROFA EMBRYO, SUS SCROFA ADRENAL GLAND, SUS SCROFA PLACENTA, SELENIUM, THUJA OCCIDENTALIS LEAFY TWIG, CONIUM MACULATUM FLOWERING TOP, ACONITUM NAPELLUS, ALOE, BARIUM OXALOSUCCINATE, SUS SCROFA CEREBRUM, ARNICA MONTANA and 2 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Feb 17, 2021 |
| 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: