NDC product
Dizzi-V
NDC 55714-4780 · Newton Laboratories, Inc.
Key facts
| Product NDC | 55714-4780 |
|---|---|
| Proprietary name | Dizzi-V |
| Nonproprietary name | Absinthium, Aconitum nap., Antimon. tart., Belladonna, Bryonia, Carbolicum acidum, Colchicum, Conium, Ferrum metallicum, Gelsemium, Glonoinum, Hyoscyamus and 15 more |
| Substances | WORMWOOD, ACONITUM NAPELLUS, ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA ROOT, PHENOL, COLCHICUM AUTUMNALE BULB, CONIUM MACULATUM FLOWERING TOP, IRON, GELSEMIUM SEMPERVIRENS ROOT, NITROGLYCERIN, HYOSCYAMUS NIGER and 15 more |
| Dosage form | PELLET |
| Route | ORAL |
| Labeler | Newton Laboratories, Inc. |
| 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], Increased IgG Production [PE] and 7 more |
| Marketing start | Sep 2, 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: