Immune Support Liquid
NDC Package 43742-1952-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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,) liquids is 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. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-1952.

Identification & Billing

NDC Package Code
43742-1952-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43742-1952
11-Digit Billing Format
43742195201

Clinical Specifications

Proprietary Name
Immune Support
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,
Substance Name
Aconitum Napellus Whole; Aristolochia Clematitis Root; Arnica Montana Whole; Arsenic Trioxide; Astragalus Propinquus Root; Baptisia Tinctoria Root; Bryonia Alba Root; Calcium Sulfide; Cortisone Acetate; Echinacea Angustifolia Whole; Eupatorium Perfoliatum Flowering Top; Euphorbia Resinifera Resin; Gelsemium Sempervirens Root; Influenza A Virus A/guangdong-maonan/swl1536/2019 Cnic-1909 (h1n1) Antigen (formaldehyde Inactivated); Influenza A Virus A/hong Kong/2671/2019 Ivr-208 (h3n2) Antigen (formaldehyde Inactivated); Influenza B Virus B/phuket/3073/2013 Antigen (formaldehyde Inactivated); Influenza B Virus B/washington/02/2019 Antigen (formaldehyde Inactivated); 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
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
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. 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.

Regulatory & Marketing

Labeler Name
Deseret Biologicals, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
05-03-2021
End Marketing Date
09-08-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43742-1952-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Immune Support, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains aconitum napellus whole; aristolochia clematitis root; arnica montana whole; arsenic trioxide; astragalus propinquus root; baptisia tinctoria root; bryonia alba root; calcium sulfide; cortisone acetate; echinacea angustifolia whole; eupatorium perfoliatum flowering top; euphorbia resinifera resin; gelsemium sempervirens root; influenza a virus a/guangdong-maonan/swl1536/2019 cnic-1909 (h1n1) antigen (formaldehyde inactivated); influenza a virus a/hong kong/2671/2019 ivr-208 (h3n2) antigen (formaldehyde inactivated); influenza b virus b/phuket/3073/2013 antigen (formaldehyde inactivated); influenza b virus b/washington/02/2019 antigen (formaldehyde inactivated); 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 as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Deseret Biologicals, Inc. on May 03, 2021.

How is this Deseret Biologicals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742195201. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
43742-1952-1
11-Digit CMS (5-4-2)
43742-1952-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.