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  4. NDC Product Code: 63479-1412 N12 Immunosode

NDC 63479-1412 N12 Immunosode

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 UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Get all the details for National Drug Code (NDC) 63479-1412 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
63479-1412
Proprietary Name:
N12 Immunosode
Product Type: [3]
Labeler Name: [5]
Apex Energetics Inc.
Labeler Code:
63479
Product Label ID:
0c54fc72-792f-0b9b-e063-6394a90ac2f0
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
12-04-1997
End Marketing Date: [10]
01-15-2024
Listing Expiration Date: [11]
01-15-2024
Exclude Flag: [12]
D
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 product labeled by Apex Energetics Inc.. The product's dosage form is . 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.

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)
  • 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)
  • SULFUR (UNII: 70FD1KFU70)
  • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
  • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
  • SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (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)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (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:

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Product Footnotes

[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.

[10] What is the End Marketing Date? - 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.

[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, 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".