Bio Immune
NDC 44911-0269

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0269?
  4. Bio Immune 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 inactivated by the FDA.

Bio Immune is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energique, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 44911-0269 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
44911-0269
Proprietary Name:
Bio Immune
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
f2a1134b-eb1c-4256-ac6c-16869d2bcf09
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
09-24-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 44911-0269?

The NDC code 44911-0269 is assigned by the FDA to the product Bio Immune. This pharmaceutical product is labeled by Energique, Inc. and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 44911-0269-1. 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?

For temporary relief of bacterial and viral conditions.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. For temporary relief of bacterial and viral conditions.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Which are the associated UNII Codes?

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

  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
  • LOBELIA INFLATA (UNII: 9PP1T3TC5U)
  • LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
  • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
  • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
  • SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
  • SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
  • SCROPHULARIA NODOSA (UNII: 7H443NUB2T)
  • SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (Active Moiety)
  • POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF)
  • POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (Active Moiety)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
  • TARAXACUM OFFICINALE (UNII: 39981FM375)
  • TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
  • VIROLA SEBIFERA RESIN (UNII: GHJ5XX5SGS)
  • VIROLA SEBIFERA RESIN (UNII: GHJ5XX5SGS) (Active Moiety)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
  • LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
  • SULFUR (UNII: 70FD1KFU70)
  • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
  • USTILAGO MAYDIS (UNII: 4K7Z7K7SWG)
  • USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (Active Moiety)
  • LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
  • LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3) (Active Moiety)
  • CANDIDA ALBICANS (UNII: 4D7G21HDBC)
  • CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
  • MILK THISTLE (UNII: U946SH95EE)
  • MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
  • CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956)
  • CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (Active Moiety)
  • AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037)
  • AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
  • LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F)
  • LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F) (Active Moiety)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N)
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
  • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • BOTULINUM TOXIN TYPE A (UNII: E211KPY694)
  • ABOBOTULINUMTOXINA (UNII: E211KPY694) (Active Moiety)
  • SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J)
  • SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J) (Active Moiety)
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
  • INFLUENZA A VIRUS (UNII: R9HH0NDE2E)
  • INFLUENZA A VIRUS (UNII: R9HH0NDE2E) (Active Moiety)
  • INFLUENZA B VIRUS (UNII: 1314JZ2X6W)
  • INFLUENZA B VIRUS (UNII: 1314JZ2X6W) (Active Moiety)
  • VACCINIA VIRUS (UNII: JDS6958QAG)
  • VACCINIA VIRUS (UNII: JDS6958QAG) (Active Moiety)
  • HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN)
  • HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (Active Moiety)
  • STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2)
  • STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (Active Moiety)
  • RANCID BEEF (UNII: 29SUH5R3HU)
  • RANCID BEEF (UNII: 29SUH5R3HU) (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)

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:

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Product & Regulatory Definitions
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".