NDC product
GUNA MATRIX DETOX
NDC 17089-460 · Guna spa
Key facts
| Product NDC | 17089-460 |
|---|---|
| Proprietary name | GUNA MATRIX DETOX |
| Nonproprietary name | sodium sulfate - podophyllum peltatum root - solidago virgaurea flowering top - apis mellifera - equisetum hyemale - strychnos nux vomica seed - hamamelis virginiana root bark stem bark - lycopodium… |
| Substances | FUCUS VESICULOSUS, SUS SCROFA VEIN, GALIUM APARINE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG, CONIUM MACULATUM FLOWERING TOP, MYOSOTIS ARVENSIS, SODIUM PYRUVATE, MALIC ACID, GRAPHITE, SILICON DIOXIDE, SODIUM SULFATE, SODIUM DIETHYL OXALACETATE and 3 more |
| Dosage form | SOLUTION/ DROPS |
| 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 | Jul 14, 2020 |
| 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: