NDC product
GUNA-STOMACH
NDC 17089-302 · Guna spa
Key facts
| Product NDC | 17089-302 |
|---|---|
| Proprietary name | GUNA-STOMACH |
| Nonproprietary name | ACTIVATED CHARCOAL - ANTIMONY TRISULFIDE - BISMUTH SUBNITRATE - DIOSCOREA VILLOSA ROOT - DOPAMINE - HUMAN EPIDERMAL GROWTH FACTOR - IPECAC - OREGANO - PICEA MARIANA RESIN - ROBINIA PSEUDOACACIA BARK… |
| Substances | PICEA MARIANA RESIN, SEMECARPUS ANACARDIUM JUICE, ANTIMONY TRISULFIDE, SILVER NITRATE, BISMUTH SUBNITRATE, ACTIVATED CHARCOAL, IPECAC, DIOSCOREA VILLOSA ROOT, DOPAMINE, HUMAN EPIDERMAL GROWTH FACTOR, MOMORDICA BALSAMINA IMMATURE FRUIT, OREGANO and 3 more |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bismuth [CS], Bismuth [EPC], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE] and 4 more |
| Marketing start | May 15, 2018 |
| 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: