NDC 43857-0500 Lymph II

Echinacea (angustifolia),Collinsonia Canadensis,Phytolacca Decandra,Kali Iodatum,Pinus - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43857-0500
Proprietary Name:
Lymph II
Non-Proprietary Name: [1]
Echinacea (angustifolia), Collinsonia Canadensis, Phytolacca Decandra, Kali Iodatum, Pinus Sylvestris, Pix Liquida, Ferrum Phosphoricum, Aesculus Hippocastanum, Baryta Carbonica, Berberis Vulgaris, Calcarea Carbonica, Calcarea Phosphorica, Causticum, Hepar Sulphuris Calcareum, Kreosotum, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Nitricum Acidum, Phosphorus, Pulsatilla (vulgaris), Silicea, Stellaria Media, Sulphur, Terebinthina, Thuja Occidentalis, Bufo Rana
Substance Name: [2]
Anemone Pulsatilla; Barium Carbonate; Berberis Vulgaris Root Bark; Bufo Bufo Cutaneous Gland; Calcium Sulfide; Causticum; Collinsonia Canadensis Root; Echinacea Angustifolia; Ferrosoferric Phosphate; Horse Chestnut; Lycopodium Clavatum Spore; Mercurius Solubilis; Nitric Acid; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Pine Tar; Pinus Sylvestris Leafy Twig; Potassium Iodide; Silicon Dioxide; Sodium Chloride; Stellaria Media; Sulfur; Thuja Occidentalis Leafy Twig; Tribasic Calcium Phosphate; Turpentine Oil; Wood Creosote
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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 Name: [5]
    Bioactive Nutritional, Inc.
    Labeler Code:
    43857
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    05-24-2019
    End Marketing Date: [10]
    07-30-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43857-0500-1

    Package Description: 60 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43857-0500?

    The NDC code 43857-0500 is assigned by the FDA to the product Lymph II which is a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Lymph II is echinacea (angustifolia), collinsonia canadensis, phytolacca decandra, kali iodatum, pinus sylvestris, pix liquida, ferrum phosphoricum, aesculus hippocastanum, baryta carbonica, berberis vulgaris, calcarea carbonica, calcarea phosphorica, causticum, hepar sulphuris calcareum, kreosotum, lycopodium clavatum, mercurius solubilis, natrum muriaticum, nitricum acidum, phosphorus, pulsatilla (vulgaris), silicea, stellaria media, sulphur, terebinthina, thuja occidentalis, bufo rana. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 43857-0500-1 60 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Lymph II?

    For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils. For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling, axillary glands swollen with soreness of the upper arm and tonsils.

    What are Lymph II Active Ingredients?

    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 Lymph II UNII Codes?

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

    Which are Lymph II Inactive Ingredients 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 for Lymph II?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] 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.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [10] 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.

    [12] 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".