NDC 43857-0397 Fng I

Echinacea (angustifolia), Lomatium Dissectum, Nasturtium Aquaticum, Tabebuia Impetiginosa, Condurango, Ginkgo Biloba, Ligusticum Porteri, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Bovine, Thymus (bovine), Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phytolacca Decandra, Sepia, Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Mucor Racemosus, Pullularia Pullulans, Rhizopus Nigricans, Torula Cerevisiae

NDC Product Code 43857-0397

NDC CODE: 43857-0397

Proprietary Name: Fng I 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: Echinacea (angustifolia), Lomatium Dissectum, Nasturtium Aquaticum, Tabebuia Impetiginosa, Condurango, Ginkgo Biloba, Ligusticum Porteri, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Bovine, Thymus (bovine), Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phytolacca Decandra, Sepia, Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Mucor Racemosus, Pullularia Pullulans, Rhizopus Nigricans, Torula Cerevisiae 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

  • 43857 - Bioactive Nutritional, Inc.

NDC 43857-0397-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Fng I with NDC 43857-0397 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Fng I is echinacea (angustifolia), lomatium dissectum, nasturtium aquaticum, tabebuia impetiginosa, condurango, ginkgo biloba, ligusticum porteri, hydrastis canadensis, propolis, glandula suprarenalis bovine, thymus (bovine), lycopodium clavatum, nux vomica, phosphoricum acidum, phytolacca decandra, sepia, alternaria tenuis nees, aspergillus niger, candida albicans, candida parapsilosis, mucor racemosus, pullularia pullulans, rhizopus nigricans, torula cerevisiae. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, 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.

Fng I 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.

  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • LOMATIUM DISSECTUM ROOT 3 [hp_X]/mL
  • NASTURTIUM OFFICINALE 3 [hp_X]/mL
  • TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
  • MARSDENIA CONDURANGO BARK 4 [hp_X]/mL
  • GINKGO 4 [hp_X]/mL
  • LIGUSTICUM PORTERI ROOT 4 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • ASTRAGALUS PROPINQUUS ROOT 6 [hp_X]/mL
  • PROPOLIS WAX 6 [hp_X]/mL
  • BOS TAURUS ADRENAL GLAND 8 [hp_X]/mL
  • BOS TAURUS THYMUS 8 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • ALTERNARIA ALTERNATA 12 [hp_X]/mL
  • ASPERGILLUS NIGER VAR. NIGER 12 [hp_X]/mL
  • CANDIDA ALBICANS 12 [hp_X]/mL
  • CANDIDA PARAPSILOSIS 12 [hp_X]/mL
  • MUCOR RACEMOSUS 12 [hp_X]/mL
  • AUREOBASIDIUM PULLULANS VAR. PULLUTANS 12 [hp_X]/mL
  • RHIZOPUS STOLONIFER 12 [hp_X]/mL
  • SACCHAROMYCES CEREVISIAE 12 [hp_X]/mL

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.
  • 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: Bioactive Nutritional, Inc.
Labeler Code: 43857
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: 06-14-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

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’.

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