NDC product
Vaccistat
NDC 44911-0633 · Energique, Inc.
Key facts
| Product NDC | 44911-0633 |
|---|---|
| Proprietary name | Vaccistat |
| Nonproprietary name | Baptisia Tinctoria, Echinacea (Angustifolia), Hydrastis Canadensis, Alumina, Antimonium Tartaricum, Mezereum, Natrum Muriaticum, Mercurius Solubilis, Silicea, Thuja Occidentalis, Malandrinum, Variolinum |
| Substances | BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, GOLDENSEAL, ALUMINUM OXIDE, ANTIMONY POTASSIUM TARTRATE, DAPHNE MEZEREUM BARK, SODIUM CHLORIDE, MERCURIUS SOLUBILIS, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG, VACCINIA VIRUS, VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | Energique, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Actively Acquired Immunity [PE], Live Vaccinia Virus Vaccine [EPC], Smallpox Vaccine [CS], Vaccines, Live, Unattenuated [CS] |
| Marketing start | Jan 4, 2021 |
| 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: