NDC product
Mytox
NDC 83027-0092 · Nutritional Specialties, Inc.
Key facts
| Product NDC | 83027-0092 |
|---|---|
| Proprietary name | Mytox |
| Nonproprietary name | Borax, Colchicum Autumnale, Drosera (Rotundifolia), Arsenicum Album, Ubidecarenonum, Agaricus Muscarius, Bufo Rana |
| Substances | SODIUM BORATE, COLCHICUM AUTUMNALE BULB, DROSERA ROTUNDIFOLIA WHOLE, ARSENIC TRIOXIDE, UBIDECARENONE, AMANITA MUSCARIA FRUITING BODY, BUFO BUFO CUTANEOUS GLAND |
| Dosage form | SPRAY |
| Route | ORAL |
| Labeler | Nutritional Specialties, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Aug 2, 2023 |
| 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: