Vaccistat Liquid
NDC Package 44911-0633-1
Package Information
Vaccistat (baptisia tinctoria, echinacea (angustifolia), hydrastis canadensis, alumina, antimonium tartaricum, mezereum, natrum muriaticum, mercurius solubilis, silicea, thuja occidentalis, malandrinum, variolinum) liquids May temporarily relieve skin irritation, dry cough, eczema, and fever.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0633.
Identification & Billing
Clinical Specifications
- ALUMINUM OXIDE 12 [hp_X]/mL
- ANTIMONY POTASSIUM TARTRATE 12 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- DAPHNE MEZEREUM BARK 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- GOLDENSEAL 6 [hp_X]/mL
- MERCURIUS SOLUBILIS 30 [hp_X]/mL
- SILICON DIOXIDE 30 [hp_X]/mL
- SODIUM CHLORIDE 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_X]/mL
- VACCINIA VIRUS 60 [hp_X]/mL
- VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN 30 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0633 - Vaccistat
- 44911-0633-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0633 - Vaccistat
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 44911-0633-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Vaccistat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains aluminum oxide; antimony potassium tartrate; baptisia tinctoria root; daphne mezereum bark; echinacea angustifolia whole; goldenseal; mercurius solubilis; silicon dioxide; sodium chloride; thuja occidentalis leafy twig; vaccinia virus; vaccinia virus strain new york city board of health live antigen as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Energique, Inc. on January 04, 2021. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911063301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.