NDC 43742-1302 Immune Support

Echinacea (angustifolia),Arnica Montana,Baptisia Tinctoria,Sanguinaria - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
43742-1302
Proprietary Name:
Immune Support
Non-Proprietary Name: [1]
Echinacea (angustifolia), Arnica Montana, Baptisia Tinctoria, Sanguinaria Canadensis, Aristolochia Clematitis, Eupatorium Perfoliatum, Euphorbium Officinarum, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (alba), Gelsemium Sempervirens, Mercurius Corrosivus, Phosphorus, Phytolacca Decandra, Pulsatilla (vulgaris), Rhus Tox, Sulphur, Thuja Occidentalis, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum, Astragalus Menziesii, Influenzinum (2017-2018), Spleen (suis), Thymus (suis)
Substance Name: [2]
Aconitum Napellus; Anemone Pulsatilla; Aristolochia Clematitis Root; Arnica Montana; Arsenic Trioxide; Astragalus Nuttallii Leaf; Baptisia Tinctoria Root; Bryonia Alba Root; Calcium Sulfide; Cortisone Acetate; Echinacea Angustifolia; Eupatorium Perfoliatum Flowering Top; Euphorbia Resinifera Resin; Gelsemium Sempervirens Root; Influenza A Virus A/singapore/gp1908/2015 Ivr-180 (h1n1) Antigen (formaldehyde Inactivated); Influenza A Virus A/singapore/infimh-16-0019/2016 Nib-104 (h3n2) Antigen (formaldehyde Inactivated); Influenza B Virus B/maryland/15/2016 Antigen (formaldehyde Inactivated); Influenza B Virus B/phuket/3073/2013 Antigen (formaldehyde Inactivated); Lachesis Muta Venom; Mercuric Chloride; Phosphorus; Phytolacca Americana Root; Rancid Beef; Sanguinaria Canadensis Root; Silver Nitrate; Sulfur; Sus Scrofa Spleen; Sus Scrofa Thymus; Thuja Occidentalis Leafy Twig; Toxicodendron Pubescens Leaf; Viscum Album Fruiting Top; Zinc
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]
    Deseret Biologicals, Inc.
    Labeler Code:
    43742
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    11-07-2018
    End Marketing Date: [10]
    04-16-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43742-1302-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43742-1302?

    The NDC code 43742-1302 is assigned by the FDA to the product Immune Support which is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Immune Support is echinacea (angustifolia), arnica montana, baptisia tinctoria, sanguinaria canadensis, aristolochia clematitis, eupatorium perfoliatum, euphorbium officinarum, aconitum napellus, argentum nitricum, arsenicum album, bryonia (alba), gelsemium sempervirens, mercurius corrosivus, phosphorus, phytolacca decandra, pulsatilla (vulgaris), rhus tox, sulphur, thuja occidentalis, hepar sulphuris calcareum, lachesis mutus, zincum metallicum, astragalus menziesii, influenzinum (2017-2018), spleen (suis), thymus (suis). 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 43742-1302-1 30 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 Immune Support?

    For temporary relief of symptoms related to infection, such as cough, fever, headache, fatigue, cold, muscle pain, sore throat, ear, nose and throat congestion.****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 infection, such as cough, fever, headache, fatigue, cold, muscle pain, sore throat, ear, nose and throat congestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Immune Support 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 Immune Support UNII Codes?

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

    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
    • ARNICA MONTANA (UNII: O80TY208ZW)
    • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
    • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
    • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
    • ARISTOLOCHIA CLEMATITIS ROOT (UNII: ZY0NX0W00D)
    • ARISTOLOCHIA CLEMATITIS ROOT (UNII: ZY0NX0W00D) (Active Moiety)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
    • EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
    • EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
    • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
    • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
    • SILVER NITRATE (UNII: 95IT3W8JZE)
    • SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
    • MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
    • MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
    • PHOSPHORUS (UNII: 27YLU75U4W)
    • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
    • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
    • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
    • ANEMONE PULSATILLA (UNII: I76KB35JEV)
    • ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
    • SULFUR (UNII: 70FD1KFU70)
    • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
    • ZINC (UNII: J41CSQ7QDS)
    • ZINC (UNII: J41CSQ7QDS) (Active Moiety)
    • ASTRAGALUS NUTTALLII LEAF (UNII: NC1P15G4KZ)
    • ASTRAGALUS NUTTALLII LEAF (UNII: NC1P15G4KZ) (Active Moiety)
    • INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: Q3P251C5MT)
    • INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180 (H1N1) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: LD80H821HF) (Active Moiety)
    • INFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 NIB-104 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 2ZSC17SIJ6)
    • INFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 NIB-104 (H3N2) HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 1R31M8U8H9) (Active Moiety)
    • INFLUENZA B VIRUS B/MARYLAND/15/2016 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 8V4458342X)
    • INFLUENZA B VIRUS B/MARYLAND/15/2016 HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: OES3CXI7E9) (Active Moiety)
    • INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: B93BQX9789)
    • INFLUENZA B VIRUS B/PHUKET/3073/2013 HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 9HB0XUS9TM) (Active Moiety)
    • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
    • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
    • SUS SCROFA THYMUS (UNII: 7B69B0BD62)
    • SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
    • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
    • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
    • CORTISONE ACETATE (UNII: 883WKN7W8X)
    • CORTISONE (UNII: V27W9254FZ) (Active Moiety)
    • RANCID BEEF (UNII: 29SUH5R3HU)
    • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)

    Which are Immune Support 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 Immune Support?

    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".