NDC product
GUNA-ALLERGY T
NDC 17089-418 · Guna spa
Key facts
| Product NDC | 17089-418 |
|---|---|
| Proprietary name | GUNA-ALLERGY T |
| Nonproprietary name | ammonium carbonate - apis mellifera - arsenic trioxide - blatta orientalis - cupric acetate - drimia maritima bulb - epinephrine - galphimia glauca flowering top - histamine dihydrochloride - luffa… |
| Substances | EPINEPHRINE, ONION, AMMONIUM CARBONATE, APIS MELLIFERA, ARSENIC TRIOXIDE, BLATTA ORIENTALIS, SUS SCROFA BRONCHUS, CUPRIC ACETATE, GALPHIMIA GLAUCA FLOWERING TOP, SUS SCROFA ADRENAL GLAND, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT and 5 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 13 more |
| Marketing start | May 27, 2010 |
| 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: