Imucode Liquid
NDC 43406-0685

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43406-0685?
  4. Imucode Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Imucode (astragalus, hydrastis, adrenalinum, thyroidinum, pituitarum posterium, arsenicum alb, baptisia, baryta carb, baryta mur, bromium, candida alb, ceanothus, chininum sulph, conium, hepar sulph calc, ignatia, indium, iodium, merc solub, phytolacca, sulphur) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Natural Creations, Inc. This medication is typically used as a adrenergic alpha-agonists [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43406-0685 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43406-0685
Proprietary Name:
Imucode
Non-Proprietary Name: [1]
Astragalus, Hydrastis, Adrenalinum, Thyroidinum, Pituitarum Posterium, Arsenicum Alb, Baptisia, Baryta Carb, Baryta Mur, Bromium, Candida Alb, Ceanothus, Chininum Sulph, Conium, Hepar Sulph Calc, Ignatia, Indium, Iodium, Merc Solub, Phytolacca, Sulphur
Substance Name: [2]
Arsenic Trioxide; Astragalus Nuttallii Leaf; Baptisia Tinctoria Whole; Barium Carbonate; Barium Chloride Dihydrate; Bromine; Calcium Sulfide; Candida Albicans; Ceanothus Americanus Leaf; Conium Maculatum Flowering Top; Epinephrine; Goldenseal; Indium; Iodine; Mercurius Solubilis; Phytolacca Americana Root; Quinine Sulfate; Strychnos Ignatii Seed; Sulfur; Sus Scrofa Pituitary Gland, Posterior; Thyroid
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Natural Creations, Inc
Labeler Code:
43406
Product Label ID:
be30901c-0673-4af0-8128-83ed59ff04b1
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
06-13-2018
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43406-0685?

The NDC code 43406-0685 is assigned by the FDA to the product Imucode. It is commonly known by its generic name, astragalus, hydrastis, adrenalinum, thyroidinum, pituitarum posterium, arsenicum alb, baptisia, baryta carb, baryta mur, bromium, candida alb, ceanothus, chininum sulph, conium, hepar sulph calc, ignatia, indium, iodium, merc solub, phytolacca, sulphur. This pharmaceutical product is labeled by Natural Creations, Inc and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43406-0685-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

USES: Temporarily relieves fever, aches & pains.**

What are Active Ingredients of this product?

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.
  • ARSENIC TRIOXIDE 30 [hp_C]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
  • ASTRAGALUS NUTTALLII LEAF 12 [hp_X]/mL
  • BAPTISIA TINCTORIA WHOLE 12 [hp_X]/mL
  • BARIUM CARBONATE 12 [hp_X]/mL
  • BARIUM CHLORIDE DIHYDRATE 12 [hp_X]/mL
  • BROMINE 12 [hp_X]/mL - A halogen with the atomic symbol Br, atomic number 35, and atomic weight 79.904. It is a volatile reddish-brown liquid that gives off suffocating vapors, is corrosive to the skin, and may cause severe gastroenteritis if ingested.
  • CALCIUM SULFIDE 12 [hp_X]/mL - RN given refers to parent cpd; see also record for lime sulfur (calcium polysulfide)
  • CANDIDA ALBICANS 30 [hp_C]/mL - A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
  • CEANOTHUS AMERICANUS LEAF 12 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
  • EPINEPHRINE 9 [hp_X]/mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
  • GOLDENSEAL 8 [hp_X]/mL
  • INDIUM 12 [hp_X]/mL - A metallic element, atomic number 49, atomic weight 114.818, symbol In. It is named from its blue line in the spectrum.
  • IODINE 12 [hp_X]/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
  • MERCURIUS SOLUBILIS 30 [hp_C]/mL
  • PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL
  • QUININE SULFATE 12 [hp_X]/mL - An alkaloid derived from the bark of the cinchona tree. It is used as an antimalarial drug, and is the active ingredient in extracts of the cinchona that have been used for that purpose since before 1633. Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose. It was used commonly and as a bitter and flavoring agent, and is still useful for the treatment of babesiosis. Quinine is also useful in some muscular disorders, especially nocturnal leg cramps and myotonia congenita, because of its direct effects on muscle membrane and sodium channels. The mechanisms of its antimalarial effects are not well understood.
  • STRYCHNOS IGNATII SEED 12 [hp_X]/mL
  • SULFUR 12 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
  • SUS SCROFA PITUITARY GLAND, POSTERIOR 9 [hp_X]/mL
  • THYROID 9 [hp_X]/mL - A highly vascularized endocrine gland consisting of two lobes joined by a thin band of tissue with one lobe on each side of the TRACHEA. It secretes THYROID HORMONES from the follicular cells and CALCITONIN from the parafollicular cells thereby regulating METABOLISM and CALCIUM level in blood, respectively.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 of this product?

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 full disclaimer at the bottom of this page.

Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".