NDC product
GUNA ARTHRO RELIEF
NDC 17089-463 · Guna spa
Key facts
| Product NDC | 17089-463 |
|---|---|
| Proprietary name | GUNA ARTHRO RELIEF |
| Nonproprietary name | arteria suis - alpha ketoglutaricum acidum - alpha lipoicum acidum - ascorbicum acidum - barium oxalsuccinicum - bryonia alba - calcarea carbonica - cartilago suis - chlorinum - cimicifuga racemosa… |
| Substances | OYSTER SHELL CALCIUM CARBONATE, CRUDE, SODIUM SULFATE, .ALPHA.-KETOGLUTARIC ACID, .ALPHA.-LIPOIC ACID, SUS SCROFA ARTERY, ASCORBIC ACID, BARIUM OXALOSUCCINATE, BRYONIA ALBA ROOT, SUS SCROFA CARTILAGE, CHLORINE, BLACK COHOSH, COLCHICUM AUTUMNALE BULB and 10 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Ascorbic Acid [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Vitamin C [EPC] |
| Marketing start | Sep 24, 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: