NDC product
Pollen-Weeds
NDC 55714-2499 · Newton Laboratories, Inc.
Key facts
| Product NDC | 55714-2499 |
|---|---|
| Proprietary name | Pollen-Weeds |
| Nonproprietary name | Ginkgo biloba, Hydrastis canadensis, Taraxacum officinale, Adrenalinum, Aletris farinosa, Alfalfa, Allium cepa, Antimonium tartaricum, Arsenicum album, Artemisia vulgaris, Baptisia tinctoria, Bellis perennis and 16 more |
| Substances | PARTHENIUM HYSTEROPHORUS, XEROPHYLLUM ASPHODELOIDES, EPINEPHRINE, ALFALFA, ALETRIS FARINOSA ROOT, ARTEMISIA VULGARIS ROOT, BELLIS PERENNIS, DYSPHANIA AMBROSIOIDES, LYCOPUS VIRGINICUS, PHYTOLACCA AMERICANA ROOT, POPULUS BALSAMIFERA LEAF BUD, POPULUS TREMULOIDES LEAF and 39 more |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Newton Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE] and 9 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: