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  4. NDC Product Code: 62713-809 Allergena Zone 9

NDC 62713-809 Allergena Zone 9

Echinacea, Baptisia Tinctoria,Hydrastis Canadensis,Myrrha,Nasturtium Aquaticum,Phytolacca - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62713-809?
  4. Allergena Zone 9 Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
62713-809
Proprietary Name:
Allergena Zone 9
Non-Proprietary Name: [1]
Echinacea, Baptisia Tinctoria, Hydrastis Canadensis, Myrrha, Nasturtium Aquaticum, Phytolacca Decandra, Trigonella Foenum-graecum, Zone 9 Tree, Zone 9 Weed, Zone 9 Grass
Substance Name: [2]
Acacia Pollen; Agrostis Gigantea Pollen; Ailanthus Altissima Pollen; Alnus Incana Subsp. Rugosa Pollen; Amaranthus Palmeri Pollen; Amaranthus Retroflexus Pollen; Ambrosia Acanthicarpa Pollen; Ambrosia Psilostachya Pollen; Atriplex Canescens Pollen; Baptisia Tinctoria Root; Bromus Inermis Pollen; Bromus Secalinus Pollen; Chenopodium Album Pollen; Cynodon Dactylon Pollen; Dactylis Glomerata Pollen; Echinacea, Unspecified; Eucalyptus Globulus Pollen; Fenugreek Leaf; Festuca Pratensis Pollen; Fraxinus Velutina Pollen; Goldenseal; Juglans Nigra Pollen; Juniperus Scopulorum Pollen; Ligustrum Vulgare Pollen; Liquidambar Styraciflua Pollen; Lolium Perenne Pollen; Morus Alba Pollen; Myrrh; Nasturtium Officinale; Olea Europaea Pollen; Phleum Pratense Pollen; Phoenix Dactylifera Pollen; Phytolacca Americana Root; Pinus Strobus Pollen; Plantago Lanceolata Pollen; Platanus Occidentalis Pollen; Poa Pratensis Pollen; Populus Deltoides Subsp. Monilifera Pollen; Prosopis Juliflora Pollen; Quercus Agrifolia Pollen; Rumex Crispus Pollen; Salix Nigra Pollen; Salsola Tragus Pollen; Sorghum Halepense Pollen; Ulmus Crassifolia Pollen; Ulmus Pumila Pollen
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Meditrend, Inc. Dba Progena Professional Formulations
    Labeler Code:
    62713
    Product Label ID:
    4c16e340-bd20-49b3-8455-81c63fa8c7ca
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-01-1987
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 62713-809-01

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    NDC Code 62713-809-02

    Package Description: 59 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 62713-809?

    The NDC code 62713-809 is assigned by the FDA to the product Allergena Zone 9 which is a human over the counter drug product labeled by Meditrend, Inc. Dba Progena Professional Formulations. The generic name of Allergena Zone 9 is echinacea, baptisia tinctoria, hydrastis canadensis, myrrha, nasturtium aquaticum, phytolacca decandra, trigonella foenum-graecum, zone 9 tree, zone 9 weed, zone 9 grass. The product's dosage form is liquid and is administered via oral form. The product is distributed in 2 packages with assigned NDC codes 62713-809-01 30 ml in 1 bottle, dropper , 62713-809-02 59 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 and RxNorm crosswalk.

    What are the uses for Allergena Zone 9?

    Use:This product is a Homeopathic Dilution formulated to support the body's immunity for the temporary relief of allergies.

    What are Allergena Zone 9 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 Allergena Zone 9 UNII Codes?

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

    • AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L)
    • AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (Active Moiety)
    • SALSOLA TRAGUS POLLEN (UNII: V174354MDI)
    • SALSOLA TRAGUS POLLEN (UNII: V174354MDI) (Active Moiety)
    • CYNODON DACTYLON POLLEN (UNII: 175F461W10)
    • CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
    • BROMUS INERMIS POLLEN (UNII: 766QT72BK6)
    • BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (Active Moiety)
    • BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046)
    • BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046) (Active Moiety)
    • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
    • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
    • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
    • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
    • FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1)
    • FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1) (Active Moiety)
    • DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P)
    • DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P) (Active Moiety)
    • LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0)
    • LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0) (Active Moiety)
    • AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA)
    • AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA) (Active Moiety)
    • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
    • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
    • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
    • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
    • BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
    • GOLDENSEAL (UNII: ZW3Z11D0JV)
    • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
    • MYRRH (UNII: JC71GJ1F3L)
    • MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
    • NASTURTIUM OFFICINALE (UNII: YH89GMV676)
    • NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
    • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
    • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
    • FENUGREEK LEAF (UNII: 487RI96K8Z)
    • FENUGREEK LEAF (UNII: 487RI96K8Z) (Active Moiety)
    • ACACIA POLLEN (UNII: 43DDR2YDYZ)
    • ACACIA POLLEN (UNII: 43DDR2YDYZ) (Active Moiety)
    • ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5)
    • ALNUS INCANA SUBSP. RUGOSA POLLEN (UNII: 605T96G8Y5) (Active Moiety)
    • FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD)
    • FRAXINUS VELUTINA POLLEN (UNII: LJT6I6Z8FD) (Active Moiety)
    • POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441)
    • POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (UNII: 5928LJ1441) (Active Moiety)
    • ULMUS CRASSIFOLIA POLLEN (UNII: G82398SD3I)
    • ULMUS CRASSIFOLIA POLLEN (UNII: G82398SD3I) (Active Moiety)
    • ULMUS PUMILA POLLEN (UNII: 030R993R8E)
    • ULMUS PUMILA POLLEN (UNII: 030R993R8E) (Active Moiety)
    • EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9)
    • EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (Active Moiety)
    • JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY)
    • JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (Active Moiety)
    • LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E)
    • LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (Active Moiety)
    • PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR)
    • PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (Active Moiety)
    • MORUS ALBA POLLEN (UNII: 3I9T68187H)
    • MORUS ALBA POLLEN (UNII: 3I9T68187H) (Active Moiety)
    • QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7)
    • QUERCUS AGRIFOLIA POLLEN (UNII: VOT5MA71M7) (Active Moiety)
    • OLEA EUROPAEA POLLEN (UNII: 43R41XZ627)
    • OLEA EUROPAEA POLLEN (UNII: 43R41XZ627) (Active Moiety)
    • PHOENIX DACTYLIFERA POLLEN (UNII: 2FV55IRB5B)
    • PHOENIX DACTYLIFERA POLLEN (UNII: 2FV55IRB5B) (Active Moiety)
    • PINUS STROBUS POLLEN (UNII: TX1ER5UV3T)
    • PINUS STROBUS POLLEN (UNII: TX1ER5UV3T) (Active Moiety)
    • LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS)
    • LIQUIDAMBAR STYRACIFLUA POLLEN (UNII: 5Q246DS5BS) (Active Moiety)
    • PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK)
    • PLATANUS OCCIDENTALIS POLLEN (UNII: E03U1K03LK) (Active Moiety)
    • AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3)
    • AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (Active Moiety)
    • JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR)
    • JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (Active Moiety)
    • SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN)
    • SALIX NIGRA POLLEN (UNII: 6M2JIH93ZN) (Active Moiety)
    • ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83)
    • ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (Active Moiety)
    • AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH)
    • AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (Active Moiety)
    • RUMEX CRISPUS POLLEN (UNII: V825XJG64G)
    • RUMEX CRISPUS POLLEN (UNII: V825XJG64G) (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)
    • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
    • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
    • AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y)
    • AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (Active Moiety)

    Which are Allergena Zone 9 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:

    Which are the Pharmacologic Classes for Allergena Zone 9?

    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.

    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.

    [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".