Allergena Hawaii, Puerto Rico And The Virgin Islands Liquid
NDC 62713-990

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 62713-990?
  4. Allergena Hawaii, Puerto Rico And The Virgin Islands Trees, Weeds And Grasses Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Allergena Hawaii, Puerto Rico And The Virgin Islands (echinacea, baptisia tinctoria, hydrastis canadensis, myrrha, phytolacca decandra, trigonella foenum-graecum, tropical tree, tropical weed, tropical grass) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Meditrend, Inc. Dba Progena Professional Formulations. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 62713-990 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
62713-990
Proprietary Name:
Allergena Hawaii, Puerto Rico And The Virgin Islands Trees, Weeds And Grasses
Non-Proprietary Name: [1]
Echinacea, Baptisia Tinctoria, Hydrastis Canadensis, Myrrha, Phytolacca Decandra, Trigonella Foenum-graecum, Tropical Tree, Tropical Weed, Tropical Grass
Substance Name: [2]
Acacia Pollen; Alnus Incana Subsp. Rugosa Pollen; Alnus Rubra Pollen; Amaranthus Retroflexus Pollen; Amaranthus Spinosus Pollen; Ambrosia Artemisiifolia Pollen; Anthoxanthum Odoratum Pollen; Artemisia Vulgaris Pollen; Baptisia Tinctoria Root; Broussonetia Papyrifera Pollen; Chenopodium Album Pollen; Cynodon Dactylon Pollen; Dactylis Glomerata Pollen; Echinacea, Unspecified; Eucalyptus Globulus Pollen; Fenugreek Leaf; Fraxinus Americana Pollen; Fraxinus Pennsylvanica Pollen; Fraxinus Velutina Pollen; Goldenseal; Juglans Nigra Pollen; Ligustrum Vulgare Pollen; Lolium Perenne Pollen; Morella Cerifera Pollen; Morus Alba Pollen; Morus Rubra Pollen; Myrrh; Paspalum Notatum Pollen; Phoenix Dactylifera Pollen; Phytolacca Americana Root; Pinus Strobus Pollen; Plantago Lanceolata Pollen; Poa Pratensis Pollen; Prosopis Juliflora Pollen; Quercus Alba Pollen; Rumex Acetosella Pollen; Rumex Crispus Pollen; Sorghum Halepense Pollen; Urtica Dioica Pollen; Xanthium Strumarium Pollen
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Meditrend, Inc. Dba Progena Professional Formulations
Labeler Code:
62713
Product Label ID:
bf625722-f8e2-40b3-b07a-5b3985a93da1
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
09-01-2024
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 62713-990?

The NDC code 62713-990 is assigned by the FDA to the product Allergena Hawaii, Puerto Rico And The Virgin Islands Trees, Weeds And Grasses. It is commonly known by its generic name, echinacea, baptisia tinctoria, hydrastis canadensis, myrrha, phytolacca decandra, trigonella foenum-graecum, tropical tree, tropical weed, tropical grass. This pharmaceutical product is labeled by Meditrend, Inc. Dba Progena Professional Formulations and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 62713-990-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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

What are Active Ingredients of this product?

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 the associated UNII Codes?

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

  • ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y)
  • ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (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)
  • 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 RUBRA POLLEN (UNII: Z0F2YK1B7H)
  • ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (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)
  • FRAXINUS PENNSYLVANICA POLLEN (UNII: 2WZG2G15WX)
  • FRAXINUS PENNSYLVANICA POLLEN (UNII: 2WZG2G15WX) (Active Moiety)
  • FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q)
  • FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (Active Moiety)
  • MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89)
  • MORELLA CERIFERA POLLEN (UNII: LC8MEV9S89) (Active Moiety)
  • EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9)
  • EUCALYPTUS GLOBULUS POLLEN (UNII: 7XW7TB10X9) (Active Moiety)
  • PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR)
  • PROSOPIS JULIFLORA POLLEN (UNII: 6EIJ3D04MR) (Active Moiety)
  • BROUSSONETIA PAPYRIFERA POLLEN (UNII: 51I6N3XIML)
  • BROUSSONETIA PAPYRIFERA POLLEN (UNII: 51I6N3XIML) (Active Moiety)
  • MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52)
  • MORUS RUBRA POLLEN (UNII: 9LYI4RTZ52) (Active Moiety)
  • MORUS ALBA POLLEN (UNII: 3I9T68187H)
  • MORUS ALBA POLLEN (UNII: 3I9T68187H) (Active Moiety)
  • QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK)
  • QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (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)
  • LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E)
  • LIGUSTRUM VULGARE POLLEN (UNII: Y3FRX92Z0E) (Active Moiety)
  • JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR)
  • JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (Active Moiety)
  • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M)
  • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (Active Moiety)
  • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW)
  • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (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)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
  • URTICA DIOICA POLLEN (UNII: DNB59M1NVU)
  • URTICA DIOICA POLLEN (UNII: DNB59M1NVU) (Active Moiety)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
  • AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N)
  • AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N) (Active Moiety)
  • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
  • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
  • AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (Active Moiety)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
  • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
  • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
  • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
  • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (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)

Which are the Inactive Ingredients associated 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 of this product?

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 full disclaimer at the bottom of this page.

Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".