NDC 43857-0436 Lymph Iii

Echinacea (angustifolia), Phytolacca Decandra, Boldo, Pinus Sylvestris, Thyroidinum (suis), Germanium Sesquioxide, Arnica Montana, Calcarea Iodata, Hamamelis Virginiana, Hepar Sulphuris Calcareum, Atp (adenosine Triphosphate Disodium), Co-enzyme Q-10, Naja Tripudians, Calcarea Phosphorica, Influenzinum, Natrum Sulphuricum, Pyrogenium, Sulphur, Carcinosin

NDC Product Code 43857-0436

NDC Code: 43857-0436

Proprietary Name: Lymph Iii 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: Echinacea (angustifolia), Phytolacca Decandra, Boldo, Pinus Sylvestris, Thyroidinum (suis), Germanium Sesquioxide, Arnica Montana, Calcarea Iodata, Hamamelis Virginiana, Hepar Sulphuris Calcareum, Atp (adenosine Triphosphate Disodium), Co-enzyme Q-10, Naja Tripudians, Calcarea Phosphorica, Influenzinum, Natrum Sulphuricum, Pyrogenium, Sulphur, Carcinosin 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

  • 43857 - Bioactive Nutritional, Inc.
    • 43857-0436 - Lymph

NDC 43857-0436-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Lymph Iii with NDC 43857-0436 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Lymph Iii is echinacea (angustifolia), phytolacca decandra, boldo, pinus sylvestris, thyroidinum (suis), germanium sesquioxide, arnica montana, calcarea iodata, hamamelis virginiana, hepar sulphuris calcareum, atp (adenosine triphosphate disodium), co-enzyme q-10, naja tripudians, calcarea phosphorica, influenzinum, natrum sulphuricum, pyrogenium, sulphur, carcinosin. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, 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.

Lymph Iii 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.

  • ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • PEUMUS BOLDUS LEAF 3 [hp_X]/mL
  • PINUS SYLVESTRIS LEAFY TWIG 6 [hp_X]/mL
  • SUS SCROFA THYROID 6 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
  • ARNICA MONTANA 12 [hp_X]/mL
  • CALCIUM IODIDE 12 [hp_X]/mL
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 12 [hp_X]/mL
  • CALCIUM SULFIDE 12 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL
  • UBIDECARENONE 12 [hp_X]/mL
  • NAJA NAJA VENOM 15 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 30 [hp_X]/mL
  • INFLUENZA A VIRUS A/CALIFORNIA/7/2009 X-181 (H1N1) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) 30 [hp_X]/mL
  • INFLUENZA A VIRUS A/HONG KONG/4801/2014 X-263B (H3N2) HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) 30 [hp_X]/mL
  • INFLUENZA B VIRUS B/BRISBANE/60/2008 HEMAGGLUTININ ANTIGEN (PROPIOLACTONE INACTIVATED) 30 [hp_X]/mL
  • SODIUM SULFATE 30 [hp_X]/mL
  • RANCID BEEF 30 [hp_X]/mL
  • SULFUR 30 [hp_X]/mL
  • HUMAN BREAST TUMOR CELL 200 [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: Bioactive Nutritional, Inc.
Labeler Code: 43857
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: 03-02-2017 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: 08-15-2022 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.

Lymph Iii Product Label Images

Lymph Iii 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:

Echinacea (Angustifolia) 1X, 12X, Phytolacca Decandra 3X, Boldo 3X, 12X, Pinus Sylvestris 6X, Thyroidinum (Suis) 6X, Germanium Sesquioxide 8X, Arnica Montana 12X, Calcarea Iodata 12X, Hamamelis Virginiana 12X, Hepar Sulphuris Calcareum 12X, ATP (Adenosine Triphosphate Disodium) 12X, 30X, Co-Enzyme Q-10 12X, 30X, Naja Tripudians 15X, Calcarea Phosphorica 30X, Influenzinum 30X, Natrum Sulphuricum 30X, Pyrogenium 30X, Sulphur 30X, Carcinosin 200X, 30C.

Indications:

For temporary relief of symptoms due to painful chronically enlarged lymph glands; exhaustion and emaciation, chronic intermittent fever with chills.

For temporary relief of symptoms due to painful chronically enlarged lymph glands; exhaustion and emaciation, chronic intermittent fever with chills.

Warnings:

If pregnant or breast-feeding, ask a health care 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:

10 drops orally, 3 times a day. 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:

BioActive HomeopathicLYMPH III2 FL OZ (60 ml)

* Please review the disclaimer below.

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