NDC product
GUNA KIDNEY PLUS
NDC 17089-474 · Guna spa
Key facts
| Product NDC | 17089-474 |
|---|---|
| Proprietary name | GUNA KIDNEY PLUS |
| Nonproprietary name | calcium sulfide - chondrodendron tomentosum root - equisetum hyemale - sus scrofa pituitary gland - apis mellifera - urtica urens - sodium chloride - lobaria pulmonaria - horse chestnut - berberis… |
| Substances | CALCIUM SULFIDE, EQUISETUM HYEMALE, SUS SCROFA PITUITARY GLAND, APIS MELLIFERA, CHONDRODENDRON TOMENTOSUM ROOT, SODIUM CHLORIDE, LOBARIA PULMONARIA, HORSE CHESTNUT, BERBERIS VULGARIS FRUIT, SOLIDAGO VIRGAUREA FLOWERING TOP, URTICA URENS |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE] and 4 more |
| Marketing start | Jan 17, 2021 |
| 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: