NDC product
EUBIOFLOR
NDC 17089-415 · Guna spa
Key facts
| Product NDC | 17089-415 |
|---|---|
| Proprietary name | EUBIOFLOR |
| Nonproprietary name | ACTIVATED CHARCOAL - AETHUSA CYNAPIUM - ALTHAEA OFFICINALIS LEAF - BILBERRY - CANDIDA ALBICANS - UNCARIA TOMENTOSA - ESCHERICHIA COLI - INDOLE - MERCURIUS SOLUBILIS - OKOUBAKA AUBREVILLEI BARK - PORK… |
| Substances | OKOUBAKA AUBREVILLEI BARK, SUS SCROFA PANCREAS, TABEBUIA IMPETIGINOSA BARK, PROTEUS VULGARIS, SKATOLE, TARAXACUM OFFICINALE, BILBERRY, VERATRUM ALBUM ROOT, MERCURIUS SOLUBILIS, AETHUSA CYNAPIUM, ALTHAEA OFFICINALIS LEAF, CANDIDA ALBICANS and 9 more |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC] and 3 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: