NDC product
GUNA-KIDNEY
NDC 17089-298 · Guna spa
Key facts
| Product NDC | 17089-298 |
|---|---|
| Proprietary name | GUNA-KIDNEY |
| Nonproprietary name | chondrodendron tomentosum root - clerodendranthus spicatus leaf - equisetum hyemale - escherichia coli - hieracium pilosella flowering top - methylene blue - nitric acid - ononis campestris - plantago… |
| Substances | ESCHERICHIA COLI, EQUISETUM HYEMALE, POTASSIUM NITRATE, PORK KIDNEY, METHYLENE BLUE, HIERACIUM PILOSELLA FLOWERING TOP, NITRIC ACID, ONONIS CAMPESTRIS, CLERODENDRANTHUS SPICATUS LEAF, CHONDRODENDRON TOMENTOSUM ROOT, PLANTAGO MAJOR, PROTEUS VULGARIS and 6 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Depigmenting Activity [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA], Oxidation-Reduction Activity [MoA], Oxidation-Reduction Agent [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: