NDC product
GUNA STOMACH PLUS
NDC 17089-477 · Guna spa
Key facts
| Product NDC | 17089-477 |
|---|---|
| Proprietary name | GUNA STOMACH PLUS |
| Nonproprietary name | Antimonium crudum - Argentum nitricum - Arsenicum album - Ipecacuanha - Nux vomica - Origanum majorana - Cuprum metallicum - Taraxacum officinale - Natrum phosphoricum - |
| Substances | STRYCHNOS NUX-VOMICA SEED, ANTIMONY TRISULFIDE, COPPER, IPECAC, SILVER NITRATE, ORIGANUM MAJORANA, TARAXACUM OFFICINALE ROOT, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, ARSENIC TRIOXIDE |
| 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], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE] and 10 more |
| Marketing start | Feb 17, 2021 |
| 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: