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  4. NDC Product Code: 43742-2140 Immune Support

NDC 43742-2140 Immune Support

Aconitum Napellus,Argentum Nitricum,Arnica Montana,Arsenicum Album,Astragalus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-2140?
  4. Immune Support Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43742-2140
Proprietary Name:
Immune Support
Non-Proprietary Name: [1]
Aconitum Napellus, Argentum Nitricum, Arnica Montana, Arsenicum Album, Astragalus Membranaceus, Baptisia Tinctoria, Bryonia (alba), Calendula Officinalis, Cortisone Aceticum, Echinacea (angustifolia), Eupatorium Perfoliatum, Euphorbium Officinarum, Gelsemium Sempervirens, Hepar Sulphuris Calcareum, Influenzinum (2023-2024), Lachesis Mutus, Mercurius Corrosivus, Phosphorus, Phytolacca Decandra, Pulsatilla (pratensis), Pyrogenium, Rhus Tox, Sanguinaria Canadensis, Spleen (suis), Sulphur, Thuja Occidentalis,
Substance Name: [2]
Aconitum Napellus Whole; Arnica Montana Whole; Arsenic Trioxide; Astragalus Mongholicus Root; Baptisia Tinctoria Root; Bryonia Alba Root; Calcium Sulfide; Calendula Officinalis Flowering Top; Cortisone Acetate; Echinacea Angustifolia Whole; Eupatorium Perfoliatum Flowering Top; Euphorbia Resinifera Resin; Gelsemium Sempervirens Root; Influenza A Virus A/darwin/6/2021 (h3n2) Whole; Influenza A Virus Whole; Influenza B Virus B/austria/1359417/2021 Bvr-26 Whole; Influenza B Virus B/phuket/3073/2013 Bvr-1b Whole; Lachesis Muta Venom; Mercuric Chloride; Phosphorus; Phytolacca Americana Root; Pulsatilla Pratensis Whole; 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
    Product Label ID:
    076d2b43-c569-4ca4-8eb0-5a2112a6414c
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    02-28-2024
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 43742-2140?

    The NDC code 43742-2140 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 aconitum napellus, argentum nitricum, arnica montana, arsenicum album, astragalus membranaceus, baptisia tinctoria, bryonia (alba), calendula officinalis, cortisone aceticum, echinacea (angustifolia), eupatorium perfoliatum, euphorbium officinarum, gelsemium sempervirens, hepar sulphuris calcareum, influenzinum (2023-2024), lachesis mutus, mercurius corrosivus, phosphorus, phytolacca decandra, pulsatilla (pratensis), pyrogenium, rhus tox, sanguinaria canadensis, spleen (suis), sulphur, thuja occidentalis, . 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 43742-2140-1 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?

    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.

    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:

    • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
    • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
    • SILVER NITRATE (UNII: 95IT3W8JZE)
    • SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
    • ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
    • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • ASTRAGALUS MONGHOLICUS ROOT (UNII: 922OP8YUPF)
    • ASTRAGALUS MONGHOLICUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
    • CORTISONE ACETATE (UNII: 883WKN7W8X)
    • CORTISONE (UNII: V27W9254FZ) (Active Moiety)
    • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (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)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (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)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (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)
    • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI)
    • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (Active Moiety)
    • RANCID BEEF (UNII: 29SUH5R3HU)
    • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
    • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
    • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
    • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
    • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
    • SULFUR (UNII: 70FD1KFU70)
    • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (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)
    • ZINC (UNII: J41CSQ7QDS)
    • ZINC (UNII: J41CSQ7QDS) (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.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [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".