Tree Antigens Liquid
NDC 44911-0545

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0545?
  4. Tree Antigens Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Tree Antigens (conium maculatum, abies canadensis, tulip gesneriana, oleander, american elm, plane (sycamore), ash, beech, willow, elder (box elder), alder, cedar, maple, hazel, poplar, silver birch, oak, hickory, arsenicum album, lycopodium clavatum, pulsatilla (pratensis), magnolia grandiflora, myrica cerifers, lilac (syringa vulgaris)) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energique, Inc.. 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 44911-0545 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
44911-0545
Proprietary Name:
Tree Antigens
Non-Proprietary Name: [1]
Conium Maculatum, Abies Canadensis, Tulip Gesneriana, Oleander, American Elm, Plane (sycamore), Ash, Beech, Willow, Elder (box Elder), Alder, Cedar, Maple, Hazel, Poplar, Silver Birch, Oak, Hickory, Arsenicum Album, Lycopodium Clavatum, Pulsatilla (pratensis), Magnolia Grandiflora, Myrica Cerifers, Lilac (syringa Vulgaris)
Substance Name: [2]
Acer Saccharum Pollen; Alnus Rubra Pollen; Arsenic Trioxide; Betula Pendula Pollen; Carya Glabra Pollen; Conium Maculatum Flowering Top; Corylus Avellana Pollen; Fagus Sylvatica Pollen; Fraxinus Excelsior Pollen; Juniperus Virginiana Pollen; Liriodendron Tulipifera Whole; Lycopodium Clavatum Spore; Magnolia Grandiflora Flower; Morella Cerifera Root Bark; Nerium Oleander Leaf; Platanus X Acerifolia Pollen; Populus Alba Pollen; Pulsatilla Pratensis Whole; Quercus Robur Pollen; Salix X Fragilis Pollen; Sambucus Canadensis Flower; Syringa Vulgaris Flower; Tsuga Canadensis Bark; Tsuga Canadensis Flower Bud; Ulmus Glabra 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]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
d0e7ee89-e66e-45e6-9a5f-47aacb9bb283
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-15-2020
End Marketing Date: [10]
09-29-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 44911-0545?

The NDC code 44911-0545 is assigned by the FDA to the product Tree Antigens. It is commonly known by its generic name, conium maculatum, abies canadensis, tulip gesneriana, oleander, american elm, plane (sycamore), ash, beech, willow, elder (box elder), alder, cedar, maple, hazel, poplar, silver birch, oak, hickory, arsenicum album, lycopodium clavatum, pulsatilla (pratensis), magnolia grandiflora, myrica cerifers, lilac (syringa vulgaris). This pharmaceutical product is labeled by Energique, Inc. 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: 44911-0545-1. 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?

May temporarily relieve symptoms associated with tree allergies, such as congestion and runny nose and sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evalutated. May temporarily relieve symptoms associated with tree allergies, such as congestion and runny nose and sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evalutated.

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:

  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
  • TSUGA CANADENSIS BARK (UNII: R53V5F950S)
  • TSUGA CANADENSIS BARK (UNII: R53V5F950S) (Active Moiety)
  • TSUGA CANADENSIS FLOWER BUD (UNII: Q3AW8FKK7X)
  • TSUGA CANADENSIS FLOWER BUD (UNII: Q3AW8FKK7X) (Active Moiety)
  • LIRIODENDRON TULIPIFERA WHOLE (UNII: 0601Z4Z0LU)
  • LIRIODENDRON TULIPIFERA WHOLE (UNII: 0601Z4Z0LU) (Active Moiety)
  • NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
  • NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI)
  • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (Active Moiety)
  • MAGNOLIA GRANDIFLORA FLOWER (UNII: RV23PE6426)
  • MAGNOLIA GRANDIFLORA FLOWER (UNII: RV23PE6426) (Active Moiety)
  • ULMUS GLABRA POLLEN (UNII: T2K08L297Q)
  • ULMUS GLABRA POLLEN (UNII: T2K08L297Q) (Active Moiety)
  • PLATANUS X ACERIFOLIA POLLEN (UNII: 77X11O684J)
  • PLATANUS X ACERIFOLIA POLLEN (UNII: 77X11O684J) (Active Moiety)
  • FRAXINUS EXCELSIOR POLLEN (UNII: 1824QUA0U3)
  • FRAXINUS EXCELSIOR POLLEN (UNII: 1824QUA0U3) (Active Moiety)
  • FAGUS SYLVATICA POLLEN (UNII: 63218N1ZBI)
  • FAGUS SYLVATICA POLLEN (UNII: 63218N1ZBI) (Active Moiety)
  • SALIX X FRAGILIS POLLEN (UNII: UQ7Z2EA3ZI)
  • SALIX X FRAGILIS POLLEN (UNII: UQ7Z2EA3ZI) (Active Moiety)
  • SAMBUCUS CANADENSIS FLOWER (UNII: C87P971T6W)
  • SAMBUCUS CANADENSIS FLOWER (UNII: C87P971T6W) (Active Moiety)
  • ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H)
  • ALNUS RUBRA POLLEN (UNII: Z0F2YK1B7H) (Active Moiety)
  • JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G)
  • JUNIPERUS VIRGINIANA POLLEN (UNII: PY0JA16R2G) (Active Moiety)
  • ACER SACCHARUM POLLEN (UNII: V38QUQ7861)
  • ACER SACCHARUM POLLEN (UNII: V38QUQ7861) (Active Moiety)
  • CORYLUS AVELLANA POLLEN (UNII: CR2J49TL6L)
  • CORYLUS AVELLANA POLLEN (UNII: CR2J49TL6L) (Active Moiety)
  • POPULUS ALBA POLLEN (UNII: VU8C8SB23P)
  • POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (Active Moiety)
  • BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y)
  • BETULA PENDULA POLLEN (UNII: ZL5TV40C5Y) (Active Moiety)
  • QUERCUS ROBUR POLLEN (UNII: 4PNW66TTHR)
  • QUERCUS ROBUR POLLEN (UNII: 4PNW66TTHR) (Active Moiety)
  • CARYA GLABRA POLLEN (UNII: KPO1Z9N98A)
  • CARYA GLABRA POLLEN (UNII: KPO1Z9N98A) (Active Moiety)
  • MORELLA CERIFERA ROOT BARK (UNII: S46HJ3710D)
  • MORELLA CERIFERA ROOT BARK (UNII: S46HJ3710D) (Active Moiety)
  • SYRINGA VULGARIS FLOWER (UNII: 9V5O040S3W)
  • SYRINGA VULGARIS FLOWER (UNII: 9V5O040S3W) (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.

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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 End Marketing Date? This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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".