NDC product
GUNA-LYMPHO
NDC 17089-291 · Guna spa
Key facts
| Product NDC | 17089-291 |
|---|---|
| Proprietary name | GUNA-LYMPHO |
| Nonproprietary name | apis mellifera - calendula officinalis flower - centella asiatica - dodecahydroxycyclohexane dihydrate - equisetum hyemale - fumaric acid - goldenseal - graphite - juglans regia leaf - levothyroxine… |
| Substances | APIS MELLIFERA, CALENDULA OFFICINALIS FLOWER, SUS SCROFA CAPILLARY TISSUE, MALIC ACID, EQUISETUM HYEMALE, FUMARIC ACID, GRAPHITE, GOLDENSEAL, CENTELLA ASIATICA, JUGLANS REGIA LEAF, LEVOTHYROXINE, SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE and 9 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 | 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: