NDC 43857-0397 Fng I
Echinacea (angustifolia),Lomatium Dissectum,Nasturtium Aquaticum,Tabebuia - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0397 - Fng
Product Packages
NDC Code 43857-0397-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43857-0397?
What are the uses for Fng I?
What are Fng I Active Ingredients?
- ALTERNARIA ALTERNATA 12 [hp_X]/mL
- ASPERGILLUS NIGER VAR. NIGER 12 [hp_X]/mL
- ASTRAGALUS PROPINQUUS ROOT 6 [hp_X]/mL
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS 12 [hp_X]/mL
- BOS TAURUS ADRENAL GLAND 8 [hp_X]/mL
- BOS TAURUS THYMUS 8 [hp_X]/mL
- CANDIDA ALBICANS 12 [hp_X]/mL - A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
- CANDIDA PARAPSILOSIS 12 [hp_X]/mL - A species of MITOSPORIC FUNGI and opportunistic pathogen associated with its ability to form BIOFILMS in catheters and parenteral nutrition IV lines. C. parapsilosis complex includes closely related species C. orthopsilosis; and C. metapsilosis.
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- GINKGO 4 [hp_X]/mL
- GOLDENSEAL 5 [hp_X]/mL
- LIGUSTICUM PORTERI ROOT 4 [hp_X]/mL
- LOMATIUM DISSECTUM ROOT 3 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MARSDENIA CONDURANGO BARK 4 [hp_X]/mL
- MUCOR RACEMOSUS 12 [hp_X]/mL
- NASTURTIUM OFFICINALE 3 [hp_X]/mL - A plant genus of the family BRASSICACEAE. Nasturtium is also used as a common name for TROPAEOLUM. The common name of watercress is also used for RORIPPA & TROPAEOLUM. This is the most popular of the edible cresses, is a hardy creeping perennial plant, native to Europe but extensively naturalized elsewhere in moist places.
- PHOSPHORIC ACID 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL
- PROPOLIS WAX 6 [hp_X]/mL
- RHIZOPUS STOLONIFER 12 [hp_X]/mL
- SACCHAROMYCES CEREVISIAE 12 [hp_X]/mL - A species of the genus SACCHAROMYCES, family Saccharomycetaceae, order Saccharomycetales, known as "baker's" or "brewer's" yeast. The dried form is used as a dietary supplement.
- SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
Which are Fng I UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N)
- LOMATIUM DISSECTUM ROOT (UNII: 5329928G5N) (Active Moiety)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
- TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX)
- TABEBUIA IMPETIGINOSA BARK (UNII: 6GLA1946WX) (Active Moiety)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- LIGUSTICUM PORTERI ROOT (UNII: 81FGO4H42J)
- LIGUSTICUM PORTERI ROOT (UNII: 81FGO4H42J) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
- ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF) (Active Moiety)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF) (Active Moiety)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N) (Active Moiety)
- MUCOR RACEMOSUS (UNII: 17RH99LQ7G)
- MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (Active Moiety)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (Active Moiety)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (Active Moiety)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (Active Moiety)
Which are Fng I 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Fng I?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Fungal Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
* Please review the disclaimer below.
[1] 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.
[2] 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.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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.
[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".