Thyrostat Liquid
NDC Package 44911-0488-1
Package Information
Thyrostat (fucus vesiculosus, spongia tosta, hypophysis suis, thyroidinum (suis), arsenicum iodatum, baryta carbonica, iodium, lycopus virginicus, natrum muriaticum) liquids May temporarily relieve difficulty swallowing, flushed face, glaring eyes, excited mental state or nervousness.****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 44911-0488.
Identification & Billing
Clinical Specifications
- ARSENIC TRIIODIDE 12 [hp_X]/mL
- BARIUM CARBONATE 12 [hp_X]/mL
- FUCUS VESICULOSUS 3 [hp_X]/mL
- IODINE 12 [hp_X]/mL
- LYCOPUS VIRGINICUS 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- SODIUM CHLORIDE 12 [hp_X]/mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL
- THYROID 6 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0488 - Thyrostat
- 44911-0488-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0488 - Thyrostat
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 44911-0488-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Thyrostat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arsenic triiodide; barium carbonate; fucus vesiculosus; iodine; lycopus virginicus; oyster shell calcium carbonate, crude; sodium chloride; spongia officinalis skeleton, roasted; sus scrofa pituitary gland; thyroid 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 February 22, 2019. 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: 44911048801. 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.