NDC product
GUNA HAY FEVER RELIEF
NDC 17089-476 · Guna spa
Key facts
| Product NDC | 17089-476 |
|---|---|
| Proprietary name | GUNA HAY FEVER RELIEF |
| Nonproprietary name | strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca… |
| Substances | STRYCHNOS NUX-VOMICA SEED, HISTAMINE DIHYDROCHLORIDE, MANGANESE, SCHOENOCAULON OFFICINALE SEED, ONION, APIS MELLIFERA, SILVER NITRATE, EUPHRASIA STRICTA, GALPHIMIA GLAUCA FLOWERING TOP, SULFUR, ARSENIC TRIOXIDE |
| Dosage form | PELLET |
| 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], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE] and 6 more |
| Marketing start | Feb 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: