NDC product
GUNA-MATRIX
NDC 17089-416 · Guna spa
Key facts
| Product NDC | 17089-416 |
|---|---|
| Proprietary name | GUNA-MATRIX |
| Nonproprietary name | ASCORBIC ACID - DODECAHYDROXYCYCLOHEXANE DIHYDRATE - FUCUS VESICULOSUS - HISTIDINE MONOHYDROCHLORIDE - HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED) - HYALURONIDASE - LACTIC ACID, DL - MALIC ACID - NADIDE - PHENYLALANINE - PRASTERONE - PROLACTIN - RANCID BEEF - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SODIUM SULFATE - SUS SCROFA CONJUNCTIVA - SUS SCROFA SMALL INTESTINE… |
| Substances | ASCORBIC ACID, SUS SCROFA CONJUNCTIVA, PRASTERONE, MALIC ACID, FUCUS VESICULOSUS, HISTIDINE MONOHYDROCHLORIDE, HYALURONIDASE, HUMAN INTERLEUKIN-6 (NONGLYCOSYLATED), LACTIC ACID, DL-, SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE, NADIDE, SODIUM DIETHYL OXALACETATE and 8 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Ascorbic Acid [CS], Endoglycosidase [EPC], Glycoside Hydrolases [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA] and 2 more |
| Marketing start | May 27, 2010 |
| 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: