Melatonin Pro Tablet
NDC Package 44911-0500-1
Package Information
Melatonin Pro (calcarea carbonica, chamomilla, cocculus indicus, coffea cruda, ferrum phosphoricum, kali phosphoricum, magnesia carbonica, melatonin, natrum muriaticum, nux vomica, pulsatilla (pratensis)) tablets May temporarily help to support healthy sleep and circadian rhythm.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a tablet delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0500.
Identification & Billing
Clinical Specifications
- ANAMIRTA COCCULUS SEED 12 [hp_X]/1
- ARABICA COFFEE BEAN 12 [hp_X]/1
- DIBASIC POTASSIUM PHOSPHATE 12 [hp_X]/1
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/1
- MAGNESIUM CARBONATE 12 [hp_X]/1
- MATRICARIA CHAMOMILLA 12 [hp_X]/1
- MELATONIN 12 [hp_X]/1
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/1
- PULSATILLA PRATENSIS WHOLE 12 [hp_X]/1
- SODIUM CHLORIDE 12 [hp_X]/1
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/1
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [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.
- 44911-0500 - Melatonin Pro
- 44911-0500-1 - 60 TABLET in 1 BOTTLE, PLASTIC
- 44911-0500 - Melatonin Pro
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 44911-0500-1 identifies a specific commercial package of 60 tablet in 1 bottle, plastic of Melatonin Pro, a human over the counter drug labeled by Energique, Inc.. This tablet is formulated for oral use and contains anamirta cocculus seed; arabica coffee bean; dibasic potassium phosphate; ferrosoferric phosphate; magnesium carbonate; matricaria chamomilla; melatonin; oyster shell calcium carbonate, crude; pulsatilla pratensis whole; sodium chloride; strychnos nux-vomica seed 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 07, 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: 44911050001. 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.