Immune Support

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 (pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum, Astragalus Membranaceus, Influenzinum (2020-2021), Spleen (suis), Thymus,


Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1952
Immune Support also known as 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 (pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum, Astragalus Membranaceus, Influenzinum (2020-2021), Spleen (suis), Thymus, is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Immune Support is 43742-1952. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Immune Support drug includes Aconitum Napellus Whole - 8 [hp_X]/mL Aristolochia Clematitis Root - 6 [hp_X]/mL Arnica Montana Whole - 4 [hp_X]/mL Arsenic Trioxide - 8 [hp_X]/mL Astragalus Propinquus Root - 12 [hp_X]/mL Baptisia Tinctoria Root - 4 [hp_X]/mL Bryonia Alba Root - 8 [hp_X]/mL Calcium Sulfide - 10 [hp_X]/mL Cortisone Acetate - 13 [hp_X]/mL Echinacea Angustifolia Whole - 1 [hp_X]/mL and more. The currest status of Immune Support drug is Active.

Drug Information:

Drug NDC: 43742-1952
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Immune Support
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: 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 (pratensis), Rhus Tox, Sulphur, Thuja Occidentalis, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum, Astragalus Membranaceus, Influenzinum (2020-2021), Spleen (suis), Thymus,
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:ACONITUM NAPELLUS WHOLE - 8 [hp_X]/mL
ARISTOLOCHIA CLEMATITIS ROOT - 6 [hp_X]/mL
ARNICA MONTANA WHOLE - 4 [hp_X]/mL
ARSENIC TRIOXIDE - 8 [hp_X]/mL
ASTRAGALUS PROPINQUUS ROOT - 12 [hp_X]/mL
BAPTISIA TINCTORIA ROOT - 4 [hp_X]/mL
BRYONIA ALBA ROOT - 8 [hp_X]/mL
CALCIUM SULFIDE - 10 [hp_X]/mL
CORTISONE ACETATE - 13 [hp_X]/mL
ECHINACEA ANGUSTIFOLIA WHOLE - 1 [hp_X]/mL
EUPATORIUM PERFOLIATUM FLOWERING TOP - 6 [hp_X]/mL
EUPHORBIA RESINIFERA RESIN - 6 [hp_X]/mL
GELSEMIUM SEMPERVIRENS ROOT - 8 [hp_X]/mL
INFLUENZA A VIRUS A/GUANGDONG-MAONAN/SWL1536/2019 CNIC-1909 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) - 12 [hp_X]/mL
INFLUENZA A VIRUS A/HONG KONG/2671/2019 IVR-208 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) - 12 [hp_X]/mL
INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE INACTIVATED) - 12 [hp_X]/mL
INFLUENZA B VIRUS B/WASHINGTON/02/2019 ANTIGEN (FORMALDEHYDE INACTIVATED) - 12 [hp_X]/mL
LACHESIS MUTA VENOM - 10 [hp_X]/mL
MERCURIC CHLORIDE - 8 [hp_X]/mL
PHOSPHORUS - 8 [hp_X]/mL
PHYTOLACCA AMERICANA ROOT - 8 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE - 8 [hp_X]/mL
RANCID BEEF - 200 [hp_X]/mL
SANGUINARIA CANADENSIS ROOT - 4 [hp_X]/mL
SILVER NITRATE - 8 [hp_X]/mL
SULFUR - 8 [hp_X]/mL
SUS SCROFA SPLEEN - 12 [hp_X]/mL
SUS SCROFA THYMUS - 12 [hp_X]/mL
THUJA OCCIDENTALIS LEAFY TWIG - 8 [hp_X]/mL
TOXICODENDRON PUBESCENS LEAF - 8 [hp_X]/mL
VISCUM ALBUM FRUITING TOP - 12 [hp_X]/mL
ZINC - 10 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 03 May, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 08 Sep, 2026
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.
Listing Expiration Date: 07 May, 2026
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UNII:U0NQ8555JD
ZY0NX0W00D
O80TY208ZW
S7V92P67HO
922OP8YUPF
5EF0HWI5WU
T7J046YI2B
1MBW07J51Q
883WKN7W8X
VB06AV5US8
1W0775VX6E
1TI1O9028K
639KR60Q1Q
NY1FF92M1E
P8ORN3UOM6
B93BQX9789
VEH9U90EHX
VSW71SS07I
53GH7MZT1R
27YLU75U4W
11E6VI8VEG
8E272251DI
29SUH5R3HU
N9288CD508
95IT3W8JZE
70FD1KFU70
92AMN5J79Y
7B69B0BD62
1NT28V9397
6IO182RP7A
BK9092J5MP
J41CSQ7QDS
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:Corticosteroid Hormone Receptor Agonists [MoA]
Corticosteroid [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
43742-1952-130 mL in 1 BOTTLE, DROPPER (43742-1952-1)03 May, 202108 Sep, 2026No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Homeopathic indications: 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 homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Immune support 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 (pratensis), rhus tox, sulphur, thuja occidentalis, hepar sulphuris calcareum, lachesis mutus, zincum metallicum, astragalus membranaceus, influenzinum (2020-2021), spleen (suis), thymus, echinacea angustifolia whole echinacea angustifolia arnica montana whole arnica montana baptisia tinctoria root baptisia tinctoria root sanguinaria canadensis root sanguinaria canadensis root aristolochia clematitis root aristolochia clematitis root eupatorium perfoliatum flowering top eupatorium perfoliatum flowering top euphorbia resinifera resin euphorbia resinifera resin aconitum napellus whole aconitum napellus silver nitrate silver cation arsenic trioxide arsenic cation (3+) bryonia alba root bryonia alba root gelsemium sempervirens root gelsemium sempervirens root mercuric chloride mercuric cation phosphorus phosphorus phytolacca americana root phytolacca americana root pulsatilla pratensis whole pulsatilla pratensis whole toxicodendron pubescens leaf toxicodendron pubescens leaf sulfur sulfur thuja occidentalis leafy twig thuja occidentalis leafy twig calcium sulfide calcium sulfide lachesis muta venom lachesis muta venom zinc zinc astragalus propinquus root astragalus propinquus root influenza a virus a/guangdong-maonan/swl1536/2019 cnic-1909 (h1n1) antigen (formaldehyde inactivated) influenza a virus a/guangdong-maonan/swl1536/2019 cnic-1909 (h1n1) hemagglutinin antigen (formaldehyde inactivated) influenza a virus a/hong kong/2671/2019 ivr-208 (h3n2) antigen (formaldehyde inactivated) influenza a virus a/hong kong/2671/2019 ivr-208 (h3n2) hemagglutinin antigen (formaldehyde inactivated) influenza b virus b/phuket/3073/2013 antigen (formaldehyde inactivated) influenza b virus b/phuket/3073/2013 bvr-1b hemagglutinin antigen (formaldehyde inactivated) influenza b virus b/washington/02/2019 antigen (formaldehyde inactivated) influenza b virus b/washington/02/2019 hemagglutinin antigen (formaldehyde inactivated) sus scrofa spleen sus scrofa spleen sus scrofa thymus sus scrofa thymus viscum album fruiting top viscum album fruiting top cortisone acetate cortisone rancid beef rancid beef water alcohol

Indications and Usage:

Homeopathic indications: 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 homeopathic principles. they have not been reviewed by the food and drug administration.

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact a physician or poison control center right away. if pregnant or breast-feeding, ask a health professional before use. tamper seal: "sealed for your protection." do not use if seal is broken or missing. warning: severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. consult a physician promptly. do not use more than two days or administer to children under 3 years of age unless directed by a physician.

Dosage and Administration:

Directions: 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.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1952-1 homeopathic immume support 1 fl oz (30 ml) immune support

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.