NDC product
GUNA-FEM
NDC 17089-231 · Guna spa
Key facts
| Product NDC | 17089-231 |
|---|---|
| Proprietary name | GUNA-FEM |
| Nonproprietary name | ADENOSINUM CICLOPHOSPHORICUM - LILIUM TIGRINUM - MELATONIN - SUS SCROFA ADRENAL GLAND - SUS SCROFA CORPUS LUTEUM - SUS SCROFA HYPOTHALAMUS - SUS SCROFA OVARY - SUS SCROFA PANCREAS - SUS SCROFA PINEAL… |
| Substances | ADENOSINE CYCLIC PHOSPHATE, SUS SCROFA CORPUS LUTEUM, SUS SCROFA ADRENAL GLAND, SUS SCROFA PITUITARY GLAND, SUS SCROFA HYPOTHALAMUS, LILIUM LANCIFOLIUM BULB, MELATONIN, SUS SCROFA OVARY, SUS SCROFA PANCREAS, SUS SCROFA PINEAL GLAND, SUS SCROFA THYMUS, THYROID |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| 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: