NDC 44911-0610 Vermiclear

Granatum, Rhamnus Purshiana, Juglans Regia, Filix Mas, Absinthium, Aesculus Hippocastanum, Arsenicum Album, Baptisia Tinctoria, Cina, Cuprum Metallicum, Ipecacuanha, Lycopodium Clavatum, Mercurius Vivus, Nux Vomica, Pulsatilla (vulgaris), Ratanhia, Rhus Tox, Sabadilla, Santoninum, Silicea, Spigelia Anthelmia, Terebinthina, Teucrium Marum

NDC Product Code 44911-0610

NDC CODE: 44911-0610

Proprietary Name: Vermiclear What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Granatum, Rhamnus Purshiana, Juglans Regia, Filix Mas, Absinthium, Aesculus Hippocastanum, Arsenicum Album, Baptisia Tinctoria, Cina, Cuprum Metallicum, Ipecacuanha, Lycopodium Clavatum, Mercurius Vivus, Nux Vomica, Pulsatilla (vulgaris), Ratanhia, Rhus Tox, Sabadilla, Santoninum, Silicea, Spigelia Anthelmia, Terebinthina, Teucrium Marum What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 44911 - Energique, Inc.

NDC 44911-0610-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Vermiclear with NDC 44911-0610 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Vermiclear is granatum, rhamnus purshiana, juglans regia, filix mas, absinthium, aesculus hippocastanum, arsenicum album, baptisia tinctoria, cina, cuprum metallicum, ipecacuanha, lycopodium clavatum, mercurius vivus, nux vomica, pulsatilla (vulgaris), ratanhia, rhus tox, sabadilla, santoninum, silicea, spigelia anthelmia, terebinthina, teucrium marum. The product's dosage form is liquid and is administered via oral form.

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Vermiclear Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • PUNICA GRANATUM ROOT BARK 3 [hp_X]/mL
  • FRANGULA PURSHIANA BARK 3 [hp_X]/mL
  • JUGLANS REGIA LEAF 5 [hp_X]/mL
  • DRYOPTERIS FILIX-MAS ROOT 7 [hp_X]/mL
  • WORMWOOD 15 [hp_X]/mL
  • HORSE CHESTNUT 15 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 [hp_X]/mL
  • BAPTISIA TINCTORIA WHOLE 15 [hp_X]/mL
  • ARTEMISIA CINA PRE-FLOWERING TOP 15 [hp_X]/mL
  • COPPER 15 [hp_X]/mL
  • IPECAC 15 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mL
  • MERCURY 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • PULSATILLA VULGARIS 15 [hp_X]/mL
  • KRAMERIA LAPPACEA ROOT 15 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 15 [hp_X]/mL
  • SCHOENOCAULON OFFICINALE SEED 15 [hp_X]/mL
  • SANTONIN 15 [hp_X]/mL
  • SILICON DIOXIDE 15 [hp_X]/mL
  • SPIGELIA ANTHELMIA WHOLE 15 [hp_X]/mL
  • TURPENTINE OIL 15 [hp_X]/mL
  • TEUCRIUM MARUM WHOLE 15 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Energique, Inc.
Labeler Code: 44911
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-21-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Vermiclear Product Label Images

Vermiclear Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

(in each drop): 4.99% of Absinthium 15X, Aesculus Hippocastanum 15X, Arsenicum Album 15X, Baptisia Tinctoria 15X, Cina 15X, Cuprum Metallicum 15X, Filix Mas 7X, Ipecacuanha 15X, Lycopodium Clavatum 15X, Mercurius Vivus 15X, Nux Vomica 15X, Pulsatilla (Vulgaris) 15X, Ratanhia 15X, Rhus Tox 15X, Sabadilla 15X, Santoninum 15X, Silicea 15X, Spigelia Anthelmia 15X,Terebinthina 15X, Teucrium Marum 15X; 0.10% of Granatum 3X, Juglans Regia 5X, Rhamnus Purshiana 3X.

Indications:

May temporarily relieve symptoms of conditions related to parasite and worm infestation, such as skin and intestinal disorders, itching, bloating, fatigue, and tendency to catch colds.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May temporarily relieve symptoms of conditions related to parasite and worm infestation, such as skin and intestinal disorders, itching, bloating, fatigue, and tendency to catch colds.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings:

If pregnant or breast-feeding, ask a health professional before use.Keep out of reach of children. In case of overdose get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose get medical help or contact a Poison Control Center right away.

Directions:

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. If symptoms persist for more than 7 days, contact your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 20% Ethanol.

Questions:

Dist. by Energique, Inc.201 Apple Blvd.Woodbine, IA 51579 800.869.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYVERMICLEAR2 fl. oz. (60 ml)

* Please review the disclaimer below.