NDC 0268-0723 Mixed Feathers

Injection, Solution Subcutaneous - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
0268-0723
Proprietary Name:
Mixed Feathers
Non-Proprietary Name: [1]
Mixed Feathers
Substance Name: [2]
Anas Platyrhynchos Feather; Anser Anser Feather; Gallus Gallus Feather
NDC Directory Status:
Non-standardized Allergenic
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Administration Route(s): [4]
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
  • Labeler Name: [5]
    Alk-abello, Inc.
    Labeler Code:
    0268
    FDA Application Number: [6]
    BLA103753
    Marketing Category: [8]
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date: [9]
    01-01-1965
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 0268-0723-10

    Package Description: 10 mL in 1 VIAL

    NDC Code 0268-0723-50

    Package Description: 53 mL in 1 VIAL

    Product Details

    What is NDC 0268-0723?

    The NDC code 0268-0723 is assigned by the FDA to the product Mixed Feathers which is a non-standardized allergenic label product labeled by Alk-abello, Inc.. The product's dosage form is injection, solution and is administered via subcutaneous form. The product is distributed in 2 packages with assigned NDC codes 0268-0723-10 10 ml in 1 vial , 0268-0723-50 53 ml in 1 vial . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Mixed Feathers?

    Hyposensitization (injection) therapy is a treatment for patients exhibiting allergic reactions to seasonal pollens, dust, molds, animal danders, various other inhalants, and in situations where the offending allergen cannot be avoided.Prior to initiation of therapy, the clinical sensitivity should be established by careful evaluation of the patient’s history confirmed by diagnostic skin testing. Hyposensitization should not be prescribed for sensitivities to allergens which can easily be avoided.

    What are Mixed Feathers 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.

    Which are Mixed Feathers UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q)
    • FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (Active Moiety)
    • BETULA NIGRA POLLEN (UNII: 93963RFO1P)
    • BETULA NIGRA POLLEN (UNII: 93963RFO1P) (Active Moiety)
    • ACER NEGUNDO POLLEN (UNII: P6K070AR8V)
    • ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (Active Moiety)
    • POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441)
    • POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (Active Moiety)
    • ULMUS AMERICANA POLLEN (UNII: 89BAT511BD)
    • ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (Active Moiety)
    • CARYA OVATA POLLEN (UNII: 54UN9R2798)
    • CARYA OVATA POLLEN (UNII: 54UN9R2798) (Active Moiety)
    • QUERCUS RUBRA POLLEN (UNII: SVW19ET93C)
    • QUERCUS RUBRA POLLEN (UNII: SVW19ET93C) (Active Moiety)
    • PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK)
    • PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (Active Moiety)
    • BLACK WALNUT (UNII: 02WM57RXZJ)
    • BLACK WALNUT (UNII: 02WM57RXZJ) (Active Moiety)
    • SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN)
    • SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (Active Moiety)
    • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M)
    • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (Active Moiety)
    • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
    • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
    • CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN)
    • CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (Active Moiety)
    • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
    • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
    • BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U)
    • BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U) (Active Moiety)
    • ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
    • ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
    • ASPERGILLUS REPENS (UNII: SQ89E6LOME)
    • ASPERGILLUS REPENS (UNII: SQ89E6LOME) (Active Moiety)
    • ASPERGILLUS FLAVUS VAR. ORYZAE (UNII: Q6Z8UK5R3G)
    • ASPERGILLUS FLAVUS VAR. ORYZAE (UNII: Q6Z8UK5R3G) (Active Moiety)
    • ASPERGILLUS TERREUS (UNII: QBN8K7055X)
    • ASPERGILLUS TERREUS (UNII: QBN8K7055X) (Active Moiety)
    • GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
    • GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
    • ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796)
    • ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (Active Moiety)
    • ANSER ANSER FEATHER (UNII: 15XI414745)
    • ANSER ANSER FEATHER (UNII: 15XI414745) (Active Moiety)

    Which are Mixed Feathers 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:

    What is the NDC to RxNorm Crosswalk for Mixed Feathers?

    RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
    • RxCUI: 1927658 - gray birch pollen extract 50 MG/ML / river birch pollen extract 50 MG/ML Injectable Solution
    • RxCUI: 1927658 - Betula nigra pollen extract 0.05 GM/ML / Betula populifolia pollen extract 0.05 GM/ML Injectable Solution
    • RxCUI: 1927658 - Betula nigra pollen extract 50 MG/ML / Betula populifolia pollen extract 50 MG/ML Injectable Solution
    • RxCUI: 966954 - Penicillium chrysogenum var. chrysogenum allergenic extract 20,000 UNT/mL Injectable Solution
    • RxCUI: 966954 - Penicillium chrysogenum var. chrysogenum allergenic extract 20000 UNT/ML Injectable Solution

    Which are the Pharmacologic Classes for Mixed Feathers?

    * Please review the disclaimer below.

    Product Footnotes

    [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".