NDC 22840-9643 Monilia Mix
Candida Albicans And Neurospora Intermedia Solution Intradermal; Percutaneous; - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 22840 - Greer Laboratories, Inc.
- 22840-9643 - Monilia Mix
Product Packages
NDC Code 22840-9643-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 22840-9643?
What are the uses for Monilia Mix?
What are Monilia Mix Active Ingredients?
- CANDIDA ALBICANS 500 [PNU]/mL - A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
- NEUROSPORA INTERMEDIA 500 [PNU]/mL
Which are Monilia Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- USTILAGO MAYDIS (UNII: 4K7Z7K7SWG)
- USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
- EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S)
- EPIDERMOPHYTON FLOCCOSUM (UNII: 6JR6JTN25S) (Active Moiety)
- CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R)
- CLADOSPORIUM SPHAEROSPERMUM (UNII: P87YCA1U8R) (Active Moiety)
- COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD)
- COCHLIOBOLUS SPICIFER (UNII: 91M9RWP3TD) (Active Moiety)
- PAECILOMYCES VARIOTII (UNII: KO7V58BY40)
- PAECILOMYCES VARIOTII (UNII: KO7V58BY40) (Active Moiety)
- TRICHODERMA HARZIANUM (UNII: CA33Q4013Q)
- TRICHODERMA HARZIANUM (UNII: CA33Q4013Q) (Active Moiety)
- TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV)
- TRICHOPHYTON MENTAGROPHYTES (UNII: 199I7J3JIV) (Active Moiety)
- GIBBERELLA FUJIKUROI (UNII: 815V716OR2)
- GIBBERELLA FUJIKUROI (UNII: 815V716OR2) (Active Moiety)
- HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A)
- HAEMATONECTRIA HAEMATOCOCCA (UNII: 7TLR512M4A) (Active Moiety)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W)
- COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (Active Moiety)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- GEOTRICHUM CANDIDUM (UNII: 5964J742O8)
- GEOTRICHUM CANDIDUM (UNII: 5964J742O8) (Active Moiety)
- GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL)
- GLIOCLADIUM VIRIDE (UNII: 8Z8C642TPL) (Active Moiety)
- MUCOR PLUMBEUS (UNII: D7401PWY6E)
- MUCOR PLUMBEUS (UNII: D7401PWY6E) (Active Moiety)
- NEUROSPORA INTERMEDIA (UNII: 2072U60DUI)
- NEUROSPORA INTERMEDIA (UNII: 2072U60DUI) (Active Moiety)
- PLEOSPORA BETAE (UNII: V58BK047ES)
- PLEOSPORA BETAE (UNII: V58BK047ES) (Active Moiety)
- MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B)
- MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (UNII: 48Z8OUT98B) (Active Moiety)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (Active Moiety)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (Active Moiety)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (Active Moiety)
- TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N)
- TRICHOPHYTON RUBRUM (UNII: 2ZAU32517N) (Active Moiety)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (Active Moiety)
- SAROCLADIUM STRICTUM (UNII: 3F36V0451W)
- SAROCLADIUM STRICTUM (UNII: 3F36V0451W) (Active Moiety)
- BOTRYTIS CINEREA (UNII: TBW53313S7)
- BOTRYTIS CINEREA (UNII: TBW53313S7) (Active Moiety)
- RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z)
- RHODOTORULA MUCILAGINOSA (UNII: 62TY3X4N9Z) (Active Moiety)
- CLADOSPORIUM HERBARUM (UNII: O64JF11198)
- CLADOSPORIUM HERBARUM (UNII: O64JF11198) (Active Moiety)
- EUROTIUM AMSTELODAMI (UNII: D932NLL87Z)
- EUROTIUM AMSTELODAMI (UNII: D932NLL87Z) (Active Moiety)
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13)
- ASPERGILLUS FLAVUS (UNII: 3J888Y9L13) (Active Moiety)
- ASPERGILLUS NIDULANS (UNII: 242A53RB80)
- ASPERGILLUS NIDULANS (UNII: 242A53RB80) (Active Moiety)
- HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815)
- HELMINTHOSPORIUM SOLANI (UNII: U6Z259H815) (Active Moiety)
- EPICOCCUM NIGRUM (UNII: 87U156LEN7)
- EPICOCCUM NIGRUM (UNII: 87U156LEN7) (Active Moiety)
- MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C)
- MUCOR CIRCINELLOIDES F. LUSITANICUS (UNII: 0J0X819B3C) (Active Moiety)
- CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A)
- CHAETOMIUM GLOBOSUM (UNII: 5016WB8B8A) (Active Moiety)
- ACREMONIUM STRICTUM (UNII: 3F36V0451W)
- ACREMONIUM STRICTUM (UNII: 3F36V0451W) (Active Moiety)
- RHIZOPUS ARRHIZUS (UNII: 8476849N1Y)
- RHIZOPUS ARRHIZUS (UNII: 8476849N1Y) (Active Moiety)
Which are Monilia Mix 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:
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Monilia Mix?
- RxCUI: 1000163 - Alternaria alternata allergenic extract 20000 UNT/ML Injectable Solution
- RxCUI: 1000163 - Alternaria alternata allergenic extract 20,000 UNT/ML Injectable Solution
- RxCUI: 1000163 - Alternaria tenuis allergenic extract 20,000 UNT/ML Injectable Solution
- RxCUI: 1006288 - Aspergillus flavus allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 1006288 - Aspergillus flavus allergenic extract 0.05 GM/ML Injectable Solution
Which are the Pharmacologic Classes for Monilia Mix?
- 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.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[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".