NDC product
GUNA-VIRUS
NDC 17089-251 · Guna spa
Key facts
| Product NDC | 17089-251 |
|---|---|
| Proprietary name | GUNA-VIRUS |
| Nonproprietary name | aldesleukin - everlasting extract - fomitopsis pinicola fruiting body - interferon gamma-1b - melatonin - metenkefalin - reishi - rice - serotonin - soybean - sus scrofa blood - sus scrofa small… |
| Substances | ALDESLEUKIN, EVERLASTING EXTRACT, FOMITOPSIS PINICOLA FRUITING BODY, INTERFERON GAMMA-1B, METENKEFALIN, REISHI, BROWN RICE, SEROTONIN, SOYBEAN, SUS SCROFA BLOOD, SUS SCROFA SPLEEN, MELATONIN and 1 more |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Lymphocyte Activation [PE] and 7 more |
| Marketing start | May 23, 2006 |
| 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: