NDC 43406-0120 Fungus Nosode
Achorion Scho,Alternaria Alt,Aspergillus Fum,Aspergillus Niger,Boletus Sat,Botrytis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43406-0120?
What are the uses for Fungus Nosode?
What are Fungus Nosode Active Ingredients?
- ALTERNARIA ALTERNATA 200 [hp_X]/mL
- ASPERGILLUS FUMIGATUS 200 [hp_X]/mL - A species of imperfect fungi from which the antibiotic fumigatin is obtained. Its spores may cause respiratory infection in birds and mammals.
- ASPERGILLUS NIGER VAR. NIGER 200 [hp_X]/mL
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS 200 [hp_X]/mL
- BOLETUS SATANAS FRUITING BODY 200 [hp_X]/mL
- BOTRYTIS CINEREA 200 [hp_X]/mL
- CANDIDA PARAPSILOSIS 200 [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.
- COCHLIOBOLUS SATIVUS 200 [hp_X]/mL
- EPIDERMOPHYTON FLOCCOSUM 200 [hp_X]/mL
- FUSARIUM OXYSPORUM 200 [hp_X]/mL
- HORTAEA WERNECKII 200 [hp_X]/mL
- RHIZOPUS STOLONIFER 200 [hp_X]/mL
- SACCHAROMYCES CEREVISIAE RNA 200 [hp_X]/mL
- TRICHOPHYTON SCHOENLEINII 200 [hp_X]/mL
- USTILAGO MAYDIS 200 [hp_X]/mL
Which are Fungus Nosode UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICHOPHYTON SCHOENLEINII (UNII: Z4MD1809H1)
- TRICHOPHYTON SCHOENLEINII (UNII: Z4MD1809H1) (Active Moiety)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- BOLETUS SATANAS FRUITING BODY (UNII: 68OG1407SM)
- BOLETUS SATANAS FRUITING BODY (UNII: 68OG1407SM) (Active Moiety)
- BOTRYTIS CINEREA (UNII: TBW53313S7)
- BOTRYTIS CINEREA (UNII: TBW53313S7) (Active Moiety)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N) (Active Moiety)
- HORTAEA WERNECKII (UNII: R0AD5705HC)
- HORTAEA WERNECKII (UNII: R0AD5705HC) (Active Moiety)
- FUSARIUM OXYSPORUM (UNII: 5398RXP8KU)
- FUSARIUM OXYSPORUM (UNII: 5398RXP8KU) (Active Moiety)
- COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W)
- COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (Active Moiety)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (Active Moiety)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (Active Moiety)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (Active Moiety)
- EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S)
- EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (Active Moiety)
- USTILAGO MAYDIS (UNII: 4K7Z7K7SWG)
- USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (Active Moiety)
Which are Fungus Nosode 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Fungus Nosode?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Fungal Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
* 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.
[11] 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.
[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".