NDC product
GUNA-LIVER
NDC 17089-311 · Guna spa
Key facts
| Product NDC | 17089-311 |
|---|---|
| Proprietary name | GUNA-LIVER |
| Nonproprietary name | CEANOTHUS AMERICANUS LEAF - CHELIDONIUM MAJUS - CHIONANTHUS VIRGINICUS BARK - CHOLINE HYDROXIDE - COBALAMIN - CULVER ROOT - FUMARIC ACID - INOSITOL - LYCOPODIUM CLAVATUM SPORE - NIACIN - PORK LIVER… |
| Substances | SILYBUM MARIANUM SEED, CEANOTHUS AMERICANUS LEAF, CHELIDONIUM MAJUS, CHIONANTHUS VIRGINICUS BARK, CHOLINE HYDROXIDE, COBALAMIN, FUMARIC ACID, SUS SCROFA GALLBLADDER, PORK LIVER, INOSITOL, SUS SCROFA JEJUNUM, POTASSIUM SULFATE and 12 more |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Nicotinic Acid [EPC], Nicotinic Acids [CS], Osmotic Activity [MoA] and 5 more |
| 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: