Lymph Liquid
NDC 43857-0641

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0641?
  4. Lymph Iii Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Lymph (echinacea (angustifolia), boldo, phytolacca decandra, pinus sylvestris, thyroidinum (suis), germanium sesquioxide, arnica montana, calcarea iodata, hamamelis virginiana, hepar sulphuris calcareum, adenosinum triphosphoricum dinatrum, ubidecarenonum, naja tripudians, calcarea phosphorica, natrum sulphuricum, pyrogenium, sulphur, carcinosin, influenzinum (2023-2024)) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bioactive Nutritional, Inc.. This medication is typically used as a blood coagulation factor [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43857-0641 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43857-0641
Proprietary Name:
Lymph Iii
Non-Proprietary Name: [1]
Echinacea (angustifolia), Boldo, Phytolacca Decandra, Pinus Sylvestris, Thyroidinum (suis), Germanium Sesquioxide, Arnica Montana, Calcarea Iodata, Hamamelis Virginiana, Hepar Sulphuris Calcareum, Adenosinum Triphosphoricum Dinatrum, Ubidecarenonum, Naja Tripudians, Calcarea Phosphorica, Natrum Sulphuricum, Pyrogenium, Sulphur, Carcinosin, Influenzinum (2023-2024)
Substance Name: [2]
Echinacea Angustifolia Whole; Peumus Boldus Leaf; Phytolacca Americana Root; Pinus Sylvestris Leafy Twig; Thyroid; Germanium Sesquioxide; Arnica Montana Whole; Calcium Iodide; Hamamelis Virginiana Root Bark/stem Bark; Calcium Sulfide; Adenosine Triphosphate Disodium; Ubidecarenone; Naja Naja Venom; Tribasic Calcium Phosphate; Sodium Sulfate; Rancid Beef; Sulfur; Human Breast Tumor Cell; Influenza A Virus Whole; Influenza A Virus A/darwin/6/2021 (h3n2) Whole; Influenza B Virus B/austria/1359417/2021 Bvr-26 Whole; Influenza B Virus B/phuket/3073/2013 Bvr-1b Whole
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
0e95e7a3-6eb5-4767-a273-028ef7a57cfa
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-22-2024
End Marketing Date: [10]
05-31-2029
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43857-0641?

The NDC code 43857-0641 is assigned by the FDA to the product Lymph Iii. It is commonly known by its generic name, echinacea (angustifolia), boldo, phytolacca decandra, pinus sylvestris, thyroidinum (suis), germanium sesquioxide, arnica montana, calcarea iodata, hamamelis virginiana, hepar sulphuris calcareum, adenosinum triphosphoricum dinatrum, ubidecarenonum, naja tripudians, calcarea phosphorica, natrum sulphuricum, pyrogenium, sulphur, carcinosin, influenzinum (2023-2024). This pharmaceutical product is labeled by Bioactive Nutritional, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43857-0641-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

What are Active Ingredients of this product?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
  • PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)
  • PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) (Active Moiety)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (Active Moiety)
  • THYROID (UNII: 6RV024OAUQ)
  • SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
  • GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T)
  • GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (Active Moiety)
  • ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • CALCIUM IODIDE (UNII: 8EKI9QEE2H)
  • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
  • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
  • ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
  • ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
  • UBIDECARENONE (UNII: EJ27X76M46)
  • UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
  • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
  • RANCID BEEF (UNII: 29SUH5R3HU)
  • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
  • SULFUR (UNII: 70FD1KFU70)
  • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
  • HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K)
  • HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K) (Active Moiety)
  • INFLUENZA A VIRUS WHOLE (UNII: R9HH0NDE2E)
  • INFLUENZA A VIRUS WHOLE (UNII: R9HH0NDE2E) (Active Moiety)
  • INFLUENZA A VIRUS A/DARWIN/6/2021 (H3N2) WHOLE (UNII: PMY5J4Z7LS)
  • INFLUENZA A VIRUS A/DARWIN/6/2021 (H3N2) WHOLE (UNII: PMY5J4Z7LS) (Active Moiety)
  • INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE (UNII: CYK5P89K8X)
  • INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE (UNII: CYK5P89K8X) (Active Moiety)
  • INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B WHOLE (UNII: PS2DCE2WVF)
  • INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B WHOLE (UNII: PS2DCE2WVF) (Active Moiety)

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

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Product & Regulatory Definitions
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.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".