NDC product
GUNA-HYPERTENSION
NDC 17089-347 · Guna spa
Key facts
| Product NDC | 17089-347 |
|---|---|
| Proprietary name | GUNA-HYPERTENSION |
| Nonproprietary name | arnica montana - fumaric acid - gold - lead - melatonin - melilotus - olea europaea flower - pork kidney - rauwolfia serpentina - sodium pyruvate - spigelia - sus scrofa adrenal gland - sus scrofa… |
| Substances | ARNICA MONTANA, GOLD, UBIDECARENONE, SUS SCROFA DIENCEPHALON, FUMARIC ACID, SUS SCROFA ADRENAL GLAND, PORK KIDNEY, MELATONIN, MELILOTUS, SODIUM PYRUVATE, OLEA EUROPAEA FLOWER, LEAD and 3 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| Marketing start | Apr 16, 2008 |
| 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: