NDC product
UNDA 1002
NDC 62106-1175 · Seroyal USA
Key facts
| Product NDC | 62106-1175 |
|---|---|
| Proprietary name | UNDA 1002 |
| Nonproprietary name | Allium sativum, Bryonia dioica, Cynara scolymus, Hamamelis virginiana, Ranunculus ficaria, Rhus toxicodendron, Sarsaparilla |
| Substances | RANUNCULUS FICARIA, SARSAPARILLA, GARLIC, CYNARA SCOLYMUS LEAF, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, TOXICODENDRON PUBESCENS SHOOT, BRYONIA DIOICA ROOT |
| 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], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS] |
| Marketing start | May 4, 2018 |
| 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: