NDC product
GUNA LYMPHO DETOX
NDC 17089-462 · Guna spa
Key facts
| Product NDC | 17089-462 |
|---|---|
| Proprietary name | GUNA LYMPHO DETOX |
| Nonproprietary name | Aesculus hippocastanum - apis mellifera - calendula officinalis flower - hexaketocyclohexane - equisetum hyemale - fumaric acid - graphite - hydrastis canadensis - hydrocotyle asiatica - juglans regia… |
| Substances | APIS MELLIFERA, CALENDULA OFFICINALIS FLOWER, MALIC ACID, EQUISETUM HYEMALE, FUMARIC ACID, GRAPHITE, JUGLANS REGIA FRUIT RIND, IMMATURE, LEVOTHYROXINE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, MYOSOTIS ARVENSIS, SODIUM DIETHYL OXALACETATE, SODIUM PYRUVATE and 8 more |
| 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], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE] and 10 more |
| 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: