Vermiclear Liquid
NDC Package 44911-0718-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Vermiclear (granatum, rhamnus purshiana, juglans regia, filix mas, absinthium, aesculus hippocastanum, arsenicum album, baptisia tinctoria, cina, cinchona officinalis, cuprum metallicum, ipecacuanha, lycopodium clavatum, mercurius vivus, nux vomica, podophyllum peltatum, pulsatilla (vulgaris), ratanhia, rhus tox, sabadilla, silicea, spigelia anthelmia, terebinthina, teucrium marum) liquids is • Adults: 30 drops (1/2 tsp.) under the tongue, 2 times daily on an empty stomach. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0718.

Identification & Billing

NDC Package Code
44911-0718-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
44911-0718
11-Digit Billing Format
44911071801

Clinical Specifications

Proprietary Name
Vermiclear
Non-Proprietary Name
Granatum, Rhamnus Purshiana, Juglans Regia, Filix Mas, Absinthium, Aesculus Hippocastanum, Arsenicum Album, Baptisia Tinctoria, Cina, Cinchona Officinalis, Cuprum Metallicum, Ipecacuanha, Lycopodium Clavatum, Mercurius Vivus, Nux Vomica, Podophyllum Peltatum, Pulsatilla (vulgaris), Ratanhia, Rhus Tox, Sabadilla, Silicea, Spigelia Anthelmia, Terebinthina, Teucrium Marum
Substance Name
Punica Granatum Root Bark; Frangula Purshiana Bark; Juglans Regia Leaf; Juglans Regia Fruit Rind, Immature; Dryopteris Filix-mas Root; Wormwood; Horse Chestnut; Arsenic Trioxide; Baptisia Tinctoria Root; Artemisia Cina Pre-flowering Top; Cinchona Officinalis Bark; Copper; Ipecac; Lycopodium Clavatum Spore; Mercury; Strychnos Nux-vomica Seed; Podophyllum; Pulsatilla Vulgaris Whole; Krameria Lappacea Root; Toxicodendron Pubescens Leaf; Schoenocaulon Officinale Seed; Silicon Dioxide; Spigelia Anthelmia Whole; Turpentine Oil; Teucrium Marum Whole
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
• Adults: 30 drops (1/2 tsp.) under the tongue, 2 times daily on an empty stomach. Children under 12: 6 drops under the tongue, 3 times daily on an empty stomach. Initial course is 4 weeks. For maintenance, take for 2 weeks every 6 months or as directed by a health care professional. • Consult a physician for use in children under 12 years of age.

Regulatory & Marketing

Labeler Name
Energique, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
08-05-2024
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 44911-0718-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Vermiclear, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains punica granatum root bark; frangula purshiana bark; juglans regia leaf; juglans regia fruit rind, immature; dryopteris filix-mas root; wormwood; horse chestnut; arsenic trioxide; baptisia tinctoria root; artemisia cina pre-flowering top; cinchona officinalis bark; copper; ipecac; lycopodium clavatum spore; mercury; strychnos nux-vomica seed; podophyllum; pulsatilla vulgaris whole; krameria lappacea root; toxicodendron pubescens leaf; schoenocaulon officinale seed; silicon dioxide; spigelia anthelmia whole; turpentine oil; teucrium marum whole 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 August 05, 2024. The current certification is valid through December 31, 2027.

How is this Energique, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911071801. 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:

10-Digit Format (5-4-1)
44911-0718-1
11-Digit CMS (5-4-2)
44911-0718-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.