1. Home
  2. Labeler Index
  3. Apex Energetics Inc.
  4. NDC Product Code: 63479-1412 N12 Immunosode

NDC 63479-1412 N12 Immunosode

Arsenic Trioxide,Baptisia Tinctoria Root,Sus Scrofa Bone Marrow,Bryonia Alba - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-1412?
  4. N12 Immunosode Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
63479-1412
Proprietary Name:
N12 Immunosode
Non-Proprietary Name: [1]
Arsenic Trioxide, Baptisia Tinctoria Root, Sus Scrofa Bone Marrow, Bryonia Alba Root, Echinacea Angustifolia, Echinacea Purpurea, Olea Europaea Flower, Ulex Europaeus, Flower, Lachesis Muta Venom, Levisticum Officinale, Treponemic Skin Canker Human
Substance Name: [2]
Arsenic Trioxide; Baptisia Tinctoria Root; Bilberry; Bryonia Alba Root; Echinacea Angustifolia; Echinacea Purpurea; Gonorrheal Urethral Secretion Human; Lachesis Muta Venom; Levisticum Officinale; Olea Europaea Flower; Rancid Beef; Salmonella Enterica Enterica Serovar Typhi; Staphylococcus Epidermidis; Staphylococcus Haemolyticus; Staphylococcus Simulans; Streptococcus Pyogenes; Sulfur; Sus Scrofa Bone Marrow; Sus Scrofa Spleen; Thuja Occidentalis Leafy Twig; Treponemic Skin Canker Human; Tuberculin Purified Protein Derivative; Ulex Europaeus Flower; Vaccinia Virus Strain New York City Board Of Health Live Antigen; Viscum Album Fruiting Top
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
  • Sublingual - Administration beneath the tongue.
  • Sublingual - Administration beneath the tongue.
    • Labeler Name: [5]
    Apex Energetics Inc.
    Labeler Code:
    63479
    Product Label ID:
    ba5fbf07-d92b-2b1d-e053-2995a90a7e52
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-15-2024
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 63479-1412?

    The NDC code 63479-1412 is assigned by the FDA to the product N12 Immunosode which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of N12 Immunosode is arsenic trioxide, baptisia tinctoria root, sus scrofa bone marrow, bryonia alba root, echinacea angustifolia, echinacea purpurea, olea europaea flower, ulex europaeus, flower, lachesis muta venom, levisticum officinale, treponemic skin canker human. The product's dosage form is solution/ drops and is administered via sublingual form. The product is distributed in 2 packages with assigned NDC codes 63479-1412-1 30 ml in 1 bottle, glass , 63479-1412-2 30 ml in 1 bottle, glass . 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 N12 Immunosode?

    Adults & children ages 12 years and over: Take 10 drops under the tongue 3-4 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

    What are N12 Immunosode 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 N12 Immunosode UNII Codes?

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

    • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
    • VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
    • SULFUR (UNII: 70FD1KFU70)
    • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
    • GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F)
    • GONORRHEAL URETHRAL SECRETION HUMAN (UNII: 9BZG9E3I8F) (Active Moiety)
    • RANCID BEEF (UNII: 29SUH5R3HU)
    • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
    • STREPTOCOCCUS PYOGENES (UNII: LJ2LP0YL98)
    • STREPTOCOCCUS PYOGENES (UNII: LJ2LP0YL98) (Active Moiety)
    • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
    • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
    • BILBERRY (UNII: 9P2U39H18W)
    • BILBERRY (UNII: 9P2U39H18W) (Active Moiety)
    • STAPHYLOCOCCUS EPIDERMIDIS (UNII: D5T403TNGE)
    • STAPHYLOCOCCUS EPIDERMIDIS (UNII: D5T403TNGE) (Active Moiety)
    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • ECHINACEA PURPUREA (UNII: QI7G114Y98)
    • ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98) (Active Moiety)
    • OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
    • OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
    • TUBERCULIN PURIFIED PROTEIN DERIVATIVE (UNII: I7L8FKN87J)
    • TUBERCULIN PURIFIED PROTEIN DERIVATIVE (UNII: I7L8FKN87J) (Active Moiety)
    • SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
    • SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)
    • VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK)
    • VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN (UNII: 4SV59689SK) (Active Moiety)
    • SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
    • SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
    • TREPONEMIC SKIN CANKER HUMAN (UNII: 4ZWP7FWI8W)
    • TREPONEMIC SKIN CANKER HUMAN (UNII: 4ZWP7FWI8W) (Active Moiety)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
    • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
    • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (Active Moiety)
    • LEVISTICUM OFFICINALE (UNII: SZD8739PH1)
    • LEVISTICUM OFFICINALE (UNII: SZD8739PH1) (Active Moiety)
    • STAPHYLOCOCCUS HAEMOLYTICUS (UNII: 092IJ99835)
    • STAPHYLOCOCCUS HAEMOLYTICUS (UNII: 092IJ99835) (Active Moiety)
    • STAPHYLOCOCCUS SIMULANS (UNII: V68E0X60VL)
    • STAPHYLOCOCCUS SIMULANS (UNII: V68E0X60VL) (Active Moiety)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
    • ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN)
    • ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN) (Active Moiety)

    Which are N12 Immunosode 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 N12 Immunosode?

    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".