NDC 43742-0859 Ebv/cfs Plus

Baptisia Tinctoria, Condurango, Echinacea (angustifolia), Ligusticum Porteri, Nasturtium Aquaticum, Phytolacca Decandra, Tabebuia Impetiginosa, Astragalus Menziesii, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Tox, Selenium Metallicum, Silicea, Epstein-barr Virus Nosode

NDC Product Code 43742-0859

NDC CODE: 43742-0859

Proprietary Name: Ebv/cfs Plus 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: Baptisia Tinctoria, Condurango, Echinacea (angustifolia), Ligusticum Porteri, Nasturtium Aquaticum, Phytolacca Decandra, Tabebuia Impetiginosa, Astragalus Menziesii, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Tox, Selenium Metallicum, Silicea, Epstein-barr Virus Nosode 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.

  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0859-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Ebv/cfs Plus with NDC 43742-0859 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Ebv/cfs Plus is baptisia tinctoria, condurango, echinacea (angustifolia), ligusticum porteri, nasturtium aquaticum, phytolacca decandra, tabebuia impetiginosa, astragalus menziesii, hydrastis canadensis, propolis, glandula suprarenalis suis, thymus (suis), aranea diadema, gelsemium sempervirens, ipecacuanha, lycopodium clavatum, mercurius solubilis, muriaticum acidum, nitricum acidum, rhus tox, selenium metallicum, silicea, epstein-barr virus nosode. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, 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.

Ebv/cfs Plus 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.

  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • MARSDENIA CONDURANGO BARK 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • LIGUSTICUM PORTERI ROOT 3 [hp_X]/mL
  • NASTURTIUM OFFICINALE 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
  • ASTRAGALUS NUTTALLII LEAF 6 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • PROPOLIS WAX 6 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • ARANEUS DIADEMATUS 12 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
  • IPECAC 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • HYDROCHLORIC ACID 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
  • SELENIUM 12 [hp_X]/mL
  • SILICON DIOXIDE 12 [hp_X]/mL
  • HUMAN HERPESVIRUS 4 30 [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: Deseret Biologicals, Inc.
Labeler Code: 43742
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: 10-03-2016 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: 09-28-2022 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.

Ebv/cfs Plus Product Label Images

Ebv/cfs Plus 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:

Baptisia Tinctoria 3X, Condurango 3X, Echinacea (Angustifolia) 3X, Ligusticum Porteri 3X, Nasturtium Aquaticum 3X, Phytolacca Decandra 3X, Tabebuia Impetiginosa 3X, Astragalus Menziesii 6X, Hydrastis Canadensis 6X, Propolis 6X, Glandula Suprarenalis Suis 8X, Thymus (Suis) 8X, Aranea Diadema 12X, Gelsemium Sempervirens 12X, Ipecacuanha 12X, Lycopodium Clavatum 12X, Mercurius Solubilis 12X, Muriaticum Acidum 12X, Nitricum Acidum 12X, Rhus Tox 12X, Selenium Metallicum 12X, Silicea 12X, Epstein-Barr Virus Nosode 30X, 60X, 200X.

Homeopathic Indications:

For temporary relief of symptoms related to Epstein-Barr Virus, fibromyalgia, or chronic fatigue syndrome including fatigue, joint pain, muscle pain, and foggy thinking.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to Epstein-Barr Virus, fibromyalgia, or chronic fatigue syndrome including fatigue, joint pain, muscle pain, and foggy thinking.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.

Directions:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-0766-1HOMEOPATHICEBV/CFSPLUS1 FL OZ (30 ml)

* Please review the disclaimer below.