NDC product
GUNA-ALLERGY-PREV
NDC 17089-299 · Guna spa
Key facts
| Product NDC | 17089-299 |
|---|---|
| Proprietary name | GUNA-ALLERGY-PREV |
| Nonproprietary name | AMBROSIA ARTEMISIIFOLIA - ANGUILLA ROSTRATA BLOOD SERUM - ARUNDO PLINIANA ROOT - BLACK CURRANT - CHELIDONIUM MAJUS - CITRIC ACID MONOHYDRATE - HISTAMINE DIHYDROCHLORIDE - HUMAN INTERLEUKIN 12… |
| Substances | AMBROSIA ARTEMISIIFOLIA, ARUNDO PLINIANA ROOT, ASCLEPIAS CURASSAVICA, BLACK CURRANT, CITRIC ACID MONOHYDRATE, HISTAMINE DIHYDROCHLORIDE, INTERFERON GAMMA-1B, HUMAN INTERLEUKIN 12, MANGANESE GLUCONATE, SODIUM PYRUVATE, SODIUM SULFATE, PARIETARIA OFFICINALIS and 7 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE] and 7 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: