NDC product
GUNA-FLU
NDC 17089-025 · Guna spa
Key facts
| Product NDC | 17089-025 |
|---|---|
| Proprietary name | GUNA-FLU |
| Nonproprietary name | ACONITUM NAPELLUS - ASCLEPIAS CURASSAVICA - ATROPA BELLADONNA - CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE - COPPER - ECHINACEA ANGUSTIFOLIA - HAEMOPHILUS INFLUENZAE TYPE B - |
| Substances | ACONITUM NAPELLUS, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE, ASCLEPIAS CURASSAVICA, ATROPA BELLADONNA, COPPER, ECHINACEA ANGUSTIFOLIA, HAEMOPHILUS INFLUENZAE TYPE B |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE] |
| 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: