NDC product
UNDA 10
NDC 62106-1109 · Seroyal USA
Key facts
| Product NDC | 62106-1109 |
|---|---|
| Proprietary name | UNDA 10 |
| Nonproprietary name | Absinthium, Argentum metallicum, Equisetum arvense, Juniperus communis, Millefolium, Rhamnus frangula |
| Substances | SILVER, EQUISETUM ARVENSE BRANCH, JUNIPER BERRY, WORMWOOD, ACHILLEA MILLEFOLIUM, FRANGULA ALNUS BARK |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Seroyal USA |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC] and 2 more |
| Marketing start | Sep 29, 2015 |
| Listing certified through | Dec 31, 2026 |
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: