NDC product
GUNA-RHINO NOSE
NDC 17089-419 · Guna spa
Key facts
| Product NDC | 17089-419 |
|---|---|
| Proprietary name | GUNA-RHINO NOSE |
| Nonproprietary name | apis mellifera - aralia racemosa root - ascorbic acid - black currant - copper - euphorbia resinifera resin - european elderberry - helianthemum canadense - histamine dihydrochloride - human… |
| Substances | ONION, APIS MELLIFERA, ARALIA RACEMOSA ROOT, SILVER NITRATE, ASCORBIC ACID, BLACK CURRANT, HELIANTHEMUM CANADENSE, COPPER, EUPHORBIA RESINIFERA RESIN, HISTAMINE DIHYDROCHLORIDE, INTERFERON GAMMA-1B, INTERLEUKIN-10 and 6 more |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Ascorbic Acid [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC] and 14 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: