NDC 44911-0376 Bio-immune

Chelidonium Majus, Lobelia Inflata, Rumex Crispus, Sambucus Nigra, Scrophularia Nodosa, Senega Officinalis, Spongia Tosta, Taraxacum Officinale, Myristica Sebifera, Sticta Pulmonaria, Sulphur, Ustilago Maidis, Polyporus Officinalis, Candida Albicans, Carduus Marianus, Crotalus Horridus, Agaricus Muscarius, Bovista Secale Cornutum, Anas Barbariae, Hepatis Et Cordis Extractum, Anthracinum, Arsenicum Album, Baptisia Tinctoria, Berberis Vulgaris, Botulinum, Dysentery Bacillus, Gaertner Bacillus (bach)

NDC Product Code 44911-0376

NDC Code: 44911-0376

Proprietary Name: Bio-immune What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Chelidonium Majus, Lobelia Inflata, Rumex Crispus, Sambucus Nigra, Scrophularia Nodosa, Senega Officinalis, Spongia Tosta, Taraxacum Officinale, Myristica Sebifera, Sticta Pulmonaria, Sulphur, Ustilago Maidis, Polyporus Officinalis, Candida Albicans, Carduus Marianus, Crotalus Horridus, Agaricus Muscarius, Bovista Secale Cornutum, Anas Barbariae, Hepatis Et Cordis Extractum, Anthracinum, Arsenicum Album, Baptisia Tinctoria, Berberis Vulgaris, Botulinum, Dysentery Bacillus, Gaertner Bacillus (bach) 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.

NDC Code Structure

  • 44911 - Energique, Inc.
    • 44911-0376 - Bio-immune

NDC 44911-0376-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bio-immune with NDC 44911-0376 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Bio-immune is chelidonium majus, lobelia inflata, rumex crispus, sambucus nigra, scrophularia nodosa, senega officinalis, spongia tosta, taraxacum officinale, myristica sebifera, sticta pulmonaria, sulphur, ustilago maidis, polyporus officinalis, candida albicans, carduus marianus, crotalus horridus, agaricus muscarius, bovista secale cornutum, anas barbariae, hepatis et cordis extractum, anthracinum, arsenicum album, baptisia tinctoria, berberis vulgaris, botulinum, dysentery bacillus, gaertner bacillus (bach). The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, Inc.

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.

Product Type: Human Otc Drug 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.

Bio-immune Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • LOBELIA INFLATA 3 [hp_X]/mL
  • RUMEX CRISPUS ROOT 3 [hp_X]/mL
  • SAMBUCUS NIGRA FLOWERING TOP 3 [hp_X]/mL
  • SCROPHULARIA NODOSA 3 [hp_X]/mL
  • POLYGALA SENEGA ROOT 3 [hp_X]/mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • VIROLA SEBIFERA RESIN 6 [hp_X]/mL
  • LOBARIA PULMONARIA 6 [hp_X]/mL
  • SULFUR 6 [hp_X]/mL
  • USTILAGO MAYDIS 6 [hp_X]/mL
  • LARICIFOMES OFFICINALIS FRUITING BODY 8 [hp_X]/mL
  • CANDIDA ALBICANS 12 [hp_X]/mL
  • MILK THISTLE 12 [hp_X]/mL
  • CROTALUS HORRIDUS HORRIDUS VENOM 12 [hp_X]/mL
  • AMANITA MUSCARIA FRUITING BODY 10 [hp_C]/mL
  • LYCOPERDON UTRIFORME FRUITING BODY 10 [hp_C]/mL
  • CLAVICEPS PURPUREA SCLEROTIUM 10 [hp_C]/mL
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 30 [hp_C]/mL
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 30 [hp_C]/mL
  • ARSENIC TRIOXIDE 30 [hp_C]/mL
  • BAPTISIA TINCTORIA ROOT 30 [hp_C]/mL
  • BERBERIS VULGARIS ROOT BARK 30 [hp_C]/mL
  • CLOSTRIDIUM BOTULINUM 30 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 30 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • INFLUENZA A VIRUS A/BRISBANE/10/2010 (H1N1) HEMAGGLUTININ ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) 30 [hp_C]/mL
  • INFLUENZA A VIRUS A/BRISBANE/10/2010 (H1N1) NEURAMINIDASE ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) 30 [hp_C]/mL
  • INFLUENZA A VIRUS A/SOUTH AUSTRALIA/55/2014 (H3N2) HEMAGGLUTININ ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) 30 [hp_C]/mL
  • INFLUENZA A VIRUS A/SOUTH AUSTRALIA/55/2014 (H3N2) NEURAMINIDASE ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) 30 [hp_C]/mL
  • INFLUENZA B VIRUS B/UTAH/9/2014 HEMAGGLUTININ ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) 30 [hp_C]/mL
  • INFLUENZA B VIRUS B/UTAH/9/2014 NEURAMINIDASE ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) 30 [hp_C]/mL
  • VACCINIA VIRUS 30 [hp_C]/mL
  • HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_C]/mL
  • STREPTOCOCCUS PNEUMONIAE 30 [hp_C]/mL
  • RANCID BEEF 30 [hp_C]/mL
  • VACCINIA VIRUS STRAIN NEW YORK CITY BOARD OF HEALTH LIVE ANTIGEN 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Energique, Inc.
Labeler Code: 44911
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 09-01-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 09-14-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Bio-immune Product Label Images

Bio-immune Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Chelidonium Majus 3X, Lobelia Inflata 3X, Rumex Crispus 3X, Sambucus Nigra 3X, Scrophularia Nodosa 3X, Senega Officinalis 3X, Spongia Tosta 3X, Taraxacum Officinale 3X, Myristica Sebifera 6X, Sticta Pulmonaria 6X, Sulphur 6X, Ustilago Maidis 6X, Polyporus Officinalis 8X, Candida Albicans 12X, Carduus Marianus 12X, Crotalus Horridus 12X, Agaricus Muscarius 10C, Bovista 10C, Secale Cornutum 10C, Anas Barbariae, Hepatis Et Cordis Extractum 30C, Anthracinum 30C, Arsenicum Album 30C, Baptisia Tinctoria 30C, Berberis Vulgaris 30C, Botulinum 30C, Dysentery Bacillus 30C, Gaertner Bacillus (Bach) 30C, Influenzinum (2015-2016) 30C, Malandrinum 30C, Pertussinum 30C, Pneumococcinum 30C, Pyrogenium 30C, Variolinum 30C.

Indications:

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.

Warnings:

If pregnant or breastfeeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in a cool, dry place.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

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

Inactive Ingredients:

Demineralized water, 20% Ethanol

Questions:

Dist. by Energique, Inc., 201 Apple Blvd.Woodbine, IA 51579     800.868.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYBIO-IMMUNE1 fl. oz. (30 ml)

* Please review the disclaimer below.

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