NDC 22840-5609 Botrytis Cinerea
Solution Intradermal; Percutaneous; Subcutaneous

Product Information

What is NDC 22840-5609?

The NDC code 22840-5609 is assigned by the FDA to the product Botrytis Cinerea which is a non-standardized allergenic label product labeled by Greer Laboratories, Inc.. The product's dosage form is solution and is administered via intradermal; percutaneous; subcutaneous form. The product is distributed in 2 packages with assigned NDC codes 22840-5609-4 50 ml in 1 vial, multi-dose , 22840-5609-5 5 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code22840-5609
Proprietary Name 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.
Botrytis Cinerea
Non-Proprietary Name 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.
Botrytis Cinerea
Product Type 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.
Non-standardized Allergenic
Dosage FormSolution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Intradermal - Administration within the dermis.
  • Percutaneous - Administration through the skin.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Greer Laboratories, Inc.
Labeler Code22840
FDA Application Number 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.
BLA101833
Marketing Category 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.
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
09-15-1981
Listing Expiration Date 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.
12-31-2024
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Botrytis Cinerea?


Product Packages

NDC Code 22840-5609-4

Package Description: 50 mL in 1 VIAL, MULTI-DOSE

NDC Code 22840-5609-5

Package Description: 5 mL in 1 BOTTLE, DROPPER

Product Details

What are Botrytis Cinerea Active Ingredients?

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.

Botrytis Cinerea Active Ingredients UNII Codes

  • 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)

Botrytis Cinerea 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.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Botrytis Cinerea Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



* Please review the disclaimer below.