NDC product
Poison Ivy
NDC 55714-2498 · Newton Laboratories, Inc.
Key facts
| Product NDC | 55714-2498 |
|---|---|
| Proprietary name | Poison Ivy |
| Nonproprietary name | Xerophyllum asphodeloides, Aconitum nap., Anacardium orientale, Apis mel., Bryonia, Cantharis, Croton, Graphites, Grindelia, Mezereum, Nux vom., Ranunc. bulb. and 7 more |
| Substances | XEROPHYLLUM ASPHODELOIDES, ACONITUM NAPELLUS, SEMECARPUS ANACARDIUM JUICE, APIS MELLIFERA, BRYONIA ALBA ROOT, LYTTA VESICATORIA, CROTON TIGLIUM SEED, GRAPHITE, GRINDELIA HIRSUTULA FLOWERING TOP, DAPHNE MEZEREUM BARK, STRYCHNOS NUX-VOMICA SEED, RANUNCULUS BULBOSUS and 7 more |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Newton Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC] and 3 more |
| Marketing start | Jan 1, 2019 |
| 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: