NDC product
GUNA ALLERGY
NDC 17089-461 · Guna spa
Key facts
| Product NDC | 17089-461 |
|---|---|
| Proprietary name | GUNA ALLERGY |
| Nonproprietary name | Adrenalinum - allium cepa - ammonium carbonicum - apis mellifica - argentum nitricum - arsenicum album - cuprum aceticum - galphimia glauca - glandula suprarenalis suis - histaminum hydrochloricum… |
| Substances | HISTAMINE DIHYDROCHLORIDE, SUS SCROFA ADRENAL GLAND, EPINEPHRINE, APIS MELLIFERA, CUPRIC ACETATE, SILVER NITRATE, DRIMIA MARITIMA BULB, GALPHIMIA GLAUCA FLOWERING TOP, SCHOENOCAULON OFFICINALE SEED, SODIUM CHLORIDE, LUFFA OPERCULATA FRUIT, MATRICARIA CHAMOMILLA WHOLE and 4 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Bee Venoms [CS], Catecholamine [EPC], Catecholamines [CS] and 9 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: