NDC product
GUNA LIVER PLUS
NDC 17089-478 · Guna spa
Key facts
| Product NDC | 17089-478 |
|---|---|
| Proprietary name | GUNA LIVER PLUS |
| Nonproprietary name | SODIUM PYRUVATE - SILYBUM MARIANUM SEED - CHELIDONIUM MAJUS - FUMARIC ACID - PORK LIVER - TARAXACUM OFFICINALE - LYCOPODIUM CLAVATUM SPORE - SODIUM SULFATE - PHOSPHORUS - BERBERIS VULGARIS ROOT BARK |
| Substances | SILYBUM MARIANUM SEED, CHELIDONIUM MAJUS, FUMARIC ACID, PORK LIVER, SODIUM PYRUVATE, LYCOPODIUM CLAVATUM SPORE, SODIUM SULFATE, PHOSPHORUS, BERBERIS VULGARIS ROOT BARK, TARAXACUM OFFICINALE |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
| 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: