NDC product
GUNA-ARTHRO
NDC 17089-304 · Guna spa
Key facts
| Product NDC | 17089-304 |
|---|---|
| Proprietary name | GUNA-ARTHRO |
| Nonproprietary name | .ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE - |
| Substances | SUS SCROFA ARTERY, ASCORBIC ACID, BARIUM OXALOSUCCINATE, BRYONIA ALBA ROOT, CALCITONIN HUMAN, SUS SCROFA CARTILAGE, CHLORINE, BLACK COHOSH, COLCHICUM AUTUMNALE BULB, SUS SCROFA CONJUNCTIVA, SOLANUM DULCAMARA FLOWER, VELAFERMIN and 15 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Ascorbic Acid [CS], Depigmenting Activity [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA], Vitamin C [EPC] |
| 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: