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  5. NDC Package Code: 44911-0522-1 Terrestristat

NDC Package 44911-0522-1 Terrestristat

Alfalfa,Avena Sativa,Fucus Vesiculosus,Aralia Quinquefolia,Natrum Carbonicum,Thyroidinum - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
44911-0522-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
44911-0522
Proprietary Name:
Terrestristat
Non-Proprietary Name:
Alfalfa, Avena Sativa, Fucus Vesiculosus, Aralia Quinquefolia, Natrum Carbonicum, Thyroidinum (suis), Pineal Gland (suis), Rhododendron Chrysanthum, Agate, Argentum Nitricum, Cadmium Iodatum, Calcarea Phosphorica, Cuprum Metallicum, Mercurius Corrosivus, Phosphoricum Acidum, Phosphorus, Quartz, Silicea, Strontium Carbonicum, Holmium Metallicum, Radium Bromatum, Tarentula Cubensis, Uranium Nitricum, X-ray
Substance Name:
Alcohol, X-ray Exposed (1000 Rad); Alfalfa; American Ginseng; Avena Sativa Flowering Top; Cadmium Iodide; Citharacanthus Spinicrus; Copper; Fucus Vesiculosus; Holmium; Mercuric Chloride; Phosphoric Acid; Phosphorus; Radium Bromide; Rhododendron Aureum Leaf; Silicon Dioxide; Silver Nitrate; Sodium Carbonate; Strontium Carbonate; Sus Scrofa Pineal Gland; Sus Scrofa Thyroid; Tribasic Calcium Phosphate; Uranyl Nitrate Hexahydrate
Usage Information:
May temporarily relieve nervousness, anxiety, restlessness, weakness, trembling, numbness, and skin eruptions and cracking.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve nervousness, anxiety, restlessness, weakness, trembling, numbness, and skin eruptions and cracking.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
11-Digit NDC Billing Format:
44911052201
Product Type:
Human Otc Drug
Labeler Name:
Energique, Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) 30 [hp_X]/mL
  • ALFALFA 3 [hp_X]/mL
  • AMERICAN GINSENG 6 [hp_X]/mL
  • AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL
  • CADMIUM IODIDE 12 [hp_X]/mL
  • CITHARACANTHUS SPINICRUS 16 [hp_X]/mL
  • COPPER 12 [hp_X]/mL
  • FUCUS VESICULOSUS 3 [hp_X]/mL
  • HOLMIUM 16 [hp_X]/mL
  • MERCURIC CHLORIDE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • RADIUM BROMIDE 16 [hp_X]/mL
  • RHODODENDRON AUREUM LEAF 10 [hp_X]/mL
  • SILICON DIOXIDE 12 [hp_X]/mL
  • SILVER NITRATE 12 [hp_X]/mL
  • SODIUM CARBONATE 6 [hp_X]/mL
  • STRONTIUM CARBONATE 12 [hp_X]/mL
  • SUS SCROFA PINEAL GLAND 8 [hp_X]/mL
  • SUS SCROFA THYROID 6 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
  • URANYL NITRATE HEXAHYDRATE 30 [hp_X]/mL
    • Pharmacologic Class(es):
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
  • Phosphate Binder - [EPC] (Established Pharmacologic Class)
  • Phosphate Chelating Activity - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    02-19-2020
    End Marketing Date:
    10-05-2026
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 44911-0522-1?

    The NDC Packaged Code 44911-0522-1 is assigned to a package of 30 ml in 1 bottle, dropper of Terrestristat, a human over the counter drug labeled by Energique, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 44911-0522 included in the NDC Directory?

    Yes, Terrestristat with product code 44911-0522 is active and included in the NDC Directory. The product was first marketed by Energique, Inc. on February 19, 2020.

    What is the 11-digit format for NDC 44911-0522-1?

    The 11-digit format is 44911052201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-144911-0522-15-4-244911-0522-01