NDC 44911-0100 Parasite Detox

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

NDC Product Code 44911-0100

NDC CODE: 44911-0100

Proprietary Name: Parasite Detox 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: Filix Mas, Granatum, Rhamnus Purhiana, Juglans Regia, Absinthium, Aesculus Hippocastanum, Arsenicum Album, Baptista Tinctoria, Cina, Cuprum Metallicum, Ipecacuanha, Lycopodium Clavatum, Mercurius Vivus, Nux Vomica, Pulsatilla (vulgaris), Ratanhia, Rhus Tox, Sabadilla, Santoninum, Silicea, Spigelia Anthelmia, 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).
  • Drug uses not available

NDC Code Structure

  • 44911 - Energique, Inc.

NDC 44911-0100-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Parasite Detox with NDC 44911-0100 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Parasite Detox is filix mas, granatum, rhamnus purhiana, juglans regia, absinthium, aesculus hippocastanum, arsenicum album, baptista tinctoria, cina, cuprum metallicum, ipecacuanha, lycopodium clavatum, mercurius vivus, nux vomica, pulsatilla (vulgaris), ratanhia, rhus tox, sabadilla, santoninum, silicea, spigelia anthelmia, 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.

Parasite Detox 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.

  • DRYOPTERIS FILIX-MAS ROOT 3 [hp_X]/mL
  • PUNICA GRANATUM ROOT BARK 3 [hp_X]/mL
  • FRANGULA PURSHIANA BARK 3 [hp_X]/mL
  • JUGLANS REGIA LEAF 5 [hp_X]/mL
  • WORMWOOD 15 [hp_X]/mL
  • HORSE CHESTNUT 15 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 1/mL
  • BAPTISIA TINCTORIA 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 15 [hp_X]/mL
  • TEUCRIUM MARUM 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.
  • 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: 09-29-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 09-15-2021 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Parasite Detox Product Label Images

Parasite Detox 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:

FILIX MAS 3X,  GRANATUM 3X,  RHAMNUS PURHIANA 3X,  JUGLANS REGIA 5X,  ABSINTHIUM 15X,  AESCULUS HIPPOCASTANUM 15X,  ARSENICUM ALBUM 15X,  BAPTISTA TINCTORIA 15X,  CINA 15X,  CUPRUM METALLICUM 15X,  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,  TEUCRIUM MARUM 15X

Indications:

For temporary relief of symptoms of conditions related to parasite and worm infestation such as skin, immune and intestinal disorder, itching, bloating and fatigue.****These statements are based upon traditional homeopathic practice. They have not been rewiewed by the Food and Drug Administration.

For temporary relief of symptoms of conditions related to parasite and worm infestation such as skin, immune and intestinal disorder, itching, bloating and fatigue.****These statements are based upon traditional homeopathic practice. They have not been rewiewed by the Food and Drug Administration.

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. 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 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 51579800.869.8078

Package Label Display:

ENERGIQUEHOMEOPATHIC REMEDYPARASITE DETOX2 fl. oz. (60 ml)  20% Ethanol

* Please review the disclaimer below.