Relaxatone Liquid
NDC Package 44911-0640-1
Package Information
Relaxatone (passiflora incarnata, scutellaria lateriflora, valeriana officinalis, arsenicum album, calcarea carbonica, coffea cruda) liquids May temporarily relieve anxiety and stress.**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 44911-0640.
Identification & Billing
Clinical Specifications
- ARABICA COFFEE BEAN 12 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 12 [hp_X]/mL
- LYCOPUS VIRGINICUS WHOLE 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- PASSIFLORA INCARNATA FLOWERING TOP 3 [hp_X]/mL
- POTASSIUM PHOSPHATE, DIBASIC 12 [hp_X]/mL
- SCUTELLARIA LATERIFLORA WHOLE 3 [hp_X]/mL
- STRYCHNOS IGNATII SEED 12 [hp_X]/mL
- VALERIAN 3 [hp_X]/mL
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0640 - Relaxatone
- 44911-0640-1 - 60 mL in 1 BOTTLE, DROPPER
- 44911-0640 - Relaxatone
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.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 44911-0640-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Relaxatone, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arabica coffee bean; arsenic trioxide; delphinium staphisagria seed; lycopus virginicus whole; oyster shell calcium carbonate, crude; passiflora incarnata flowering top; potassium phosphate, dibasic; scutellaria lateriflora whole; strychnos ignatii seed; valerian 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 June 22, 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: 44911064001. 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.