Systemistat Liquid
NDC Package 44911-0449-1
Package Information
Systemistat (berberis vulgaris, chelidonium majus, lappa major, hydrastis canadensis, hepar sulphuris calcareum, lycopodium clavatum, sulphur, calcarea carbonica, mercurius solubilis, thuja occidentalis) liquids May temporarily relieve painless, clay colored diarrhea, eczema with itching, and burning hay fever with offensive discharge running from the nose.****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 44911-0449.
Identification & Billing
Clinical Specifications
- ARCTIUM LAPPA ROOT 3 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- CALCIUM SULFIDE 12 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 3 [hp_X]/mL
- GOLDENSEAL 5 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MERCURIUS SOLUBILIS 30 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/mL
- SULFUR 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0449 - Systemistat
- 44911-0449-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0449 - Systemistat
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 44911-0449-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Systemistat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arctium lappa root; berberis vulgaris root bark; calcium sulfide; chelidonium majus whole; goldenseal; lycopodium clavatum spore; mercurius solubilis; oyster shell calcium carbonate, crude; sulfur; thuja occidentalis leafy twig 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 March 06, 2018. 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: 44911044901. 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.