NDC product
GUNA-DERMO
NDC 17089-295 · Guna spa
Key facts
| Product NDC | 17089-295 |
|---|---|
| Proprietary name | GUNA-DERMO |
| Nonproprietary name | ALDESLEUKIN - ARSENIC TRIOXIDE - ATROPA BELLADONNA - CANAKINUMAB - ECHINACEA ANGUSTIFOLIA - GRAPHITE - MELATONIN - PLANTAGO MAJOR - SOLANUM DULCAMARA FLOWER - SULFUR - |
| Substances | ALDESLEUKIN, ARSENIC TRIOXIDE, ATROPA BELLADONNA, CANAKINUMAB, ECHINACEA ANGUSTIFOLIA, GRAPHITE, MELATONIN, PLANTAGO MAJOR, SOLANUM DULCAMARA FLOWER, SULFUR |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Increased Lymphocyte Activation [PE], Increased Lymphocyte Cell Production [PE], Interleukin-2 [CS], Lymphocyte Growth Factor [EPC] |
| 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: