Bio Immune Liquid
NDC 44911-0746

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0746?
  4. Bio Immune Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Bio Immune (chelidonium majus, lobelia inflata, rumex crispus, sambucus nigra, senega officinalis, spongia tosta, taraxacum officinale, myristica sebifera, sticta pulmonaria, sulphur, ustilago maidis, polyporus officinalis, candida albicans, carduus marianus, crotalus horridus, scrophularia nodosa, agaricus muscarius, bovista, secale cornutum, anas barbariae, hepatis et cordis extractum, anthracinum, arsenicum album, baptisia tinctoria, berberis vulgaris, botulinum, bryonia (alba), camphora, cinchona officinalis,) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energique, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 44911-0746 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
44911-0746
Proprietary Name:
Bio Immune
Non-Proprietary Name: [1]
Chelidonium Majus, Lobelia Inflata, Rumex Crispus, Sambucus Nigra, Senega Officinalis, Spongia Tosta, Taraxacum Officinale, Myristica Sebifera, Sticta Pulmonaria, Sulphur, Ustilago Maidis, Polyporus Officinalis, Candida Albicans, Carduus Marianus, Crotalus Horridus, Scrophularia Nodosa, Agaricus Muscarius, Bovista, Secale Cornutum, Anas Barbariae, Hepatis Et Cordis Extractum, Anthracinum, Arsenicum Album, Baptisia Tinctoria, Berberis Vulgaris, Botulinum, Bryonia (alba), Camphora, Cinchona Officinalis,
Substance Name: [2]
Amanita Muscaria Fruiting Body; Arsenic Trioxide; Bacillus Anthracis Immunoserum Rabbit; Baptisia Tinctoria Root; Berberis Vulgaris Root Bark; Bryonia Alba Root; Cairina Moschata Heart/liver Autolysate; Camphor (natural); Candida Albicans; Chelidonium Majus Whole; Cinchona Officinalis Bark; Claviceps Purpurea Sclerotium; Clostridium Botulinum; Crotalus Horridus Horridus Venom; Gelsemium Sempervirens Root; Human Sputum, Bordetella Pertussis Infected; Influenza A Virus A/thailand/8/2022 Ivr-237 (h3n2) Antigen (formaldehyde Inactivated); Influenza A Virus A/victoria/4897/2022 Ivr-238 (h1n1) Antigen (formaldehyde Inactivated); Influenza B Virus B/austria/1359417/2021 Bvr-26 Whole; Influenza B Virus B/phuket/3073/2013 Bvr-1b Whole; Laricifomes Officinalis Fruiting Body; Lobaria Pulmonaria; Lobelia Inflata Whole; Lycoperdon Utriforme Fruiting Body; Milk Thistle; Polygala Senega Root; Rancid Beef; Rumex Crispus Root; Salmonella Enterica Enterica Serovar Enteritidis; Sambucus Nigra Flowering Top; Scrophularia Nodosa Whole; Shigella Dysenteriae; Spongia Officinalis Skeleton, Roasted; Streptococcus Pneumoniae; Sulfur; Taraxacum Officinale; Ustilago Maydis; Vaccinia Virus; Variola Virus; Virola Sebifera Resin
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]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
fc837264-8edd-4234-a4c7-d699fcf1b8a0
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
01-08-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 44911-0746?

The NDC code 44911-0746 is assigned by the FDA to the product Bio Immune. It is commonly known by its generic name, chelidonium majus, lobelia inflata, rumex crispus, sambucus nigra, senega officinalis, spongia tosta, taraxacum officinale, myristica sebifera, sticta pulmonaria, sulphur, ustilago maidis, polyporus officinalis, candida albicans, carduus marianus, crotalus horridus, scrophularia nodosa, agaricus muscarius, bovista, secale cornutum, anas barbariae, hepatis et cordis extractum, anthracinum, arsenicum album, baptisia tinctoria, berberis vulgaris, botulinum, bryonia (alba), camphora, cinchona officinalis, . This pharmaceutical product is labeled by Energique, 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: 44911-0746-1. 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?

Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

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.

Which are the associated UNII Codes?

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

  • CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
  • CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
  • LOBELIA INFLATA WHOLE (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)
  • 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)
  • SCROPHULARIA NODOSA WHOLE (UNII: 7H443NUB2T)
  • SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (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)
  • CLOSTRIDIUM BOTULINUM (UNII: 0296055VE0)
  • CLOSTRIDIUM BOTULINUM (UNII: 0296055VE0) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • CAMPHOR (NATURAL) (UNII: N20HL7Q941)
  • CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
  • CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
  • CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
  • SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J)
  • SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J) (Active Moiety)
  • SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
  • SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: AU5C98U4BB)
  • INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: AU5C98U4BB) (Active Moiety)
  • INFLUENZA A VIRUS A/THAILAND/8/2022 IVR-237 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 6TU4EY6UNW)
  • INFLUENZA A VIRUS A/THAILAND/8/2022 IVR-237 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 6TU4EY6UNW) (Active Moiety)
  • INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE (UNII: CYK5P89K8X)
  • INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 WHOLE (UNII: CYK5P89K8X) (Active Moiety)
  • INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B WHOLE (UNII: PS2DCE2WVF)
  • INFLUENZA B VIRUS B/PHUKET/3073/2013 BVR-1B WHOLE (UNII: PS2DCE2WVF) (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)
  • VARIOLA VIRUS (UNII: 7J6DBS5FRN)
  • VARIOLA VIRUS (UNII: 7J6DBS5FRN) (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:

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.

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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".