Weed Grass Antigens Liquid
NDC 44911-0547

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0547?
  4. Weed Grass Antigens Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Weed Grass Antigens (allium cepa, arsenicum album, natrum muriaticum, nux vomica, pulsatilla (pratensis), abrotanum (artemisia abrotanum), absinthium, agrimonia eupatoria, flos, alfalfa, ambrosia artemisiaefolia, arundo mauritanica, bambusa arundinacea, cichorium intybus, flos, kentucky bluegrass, orchard grass, bermuda grass, johnson grass, rye grass, vernal grass, bahia grass, timothy grass, rumex crispus, sabadilla, sinapis arvensis, flos, solidago virgaurea, taraxacum officinale, trifolium pratense, trifolium repens,) 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 44911-0547 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
44911-0547
Proprietary Name:
Weed Grass Antigens
Non-Proprietary Name: [1]
Allium Cepa, Arsenicum Album, Natrum Muriaticum, Nux Vomica, Pulsatilla (pratensis), Abrotanum (artemisia Abrotanum), Absinthium, Agrimonia Eupatoria, Flos, Alfalfa, Ambrosia Artemisiaefolia, Arundo Mauritanica, Bambusa Arundinacea, Cichorium Intybus, Flos, Kentucky Bluegrass, Orchard Grass, Bermuda Grass, Johnson Grass, Rye Grass, Vernal Grass, Bahia Grass, Timothy Grass, Rumex Crispus, Sabadilla, Sinapis Arvensis, Flos, Solidago Virgaurea, Taraxacum Officinale, Trifolium Pratense, Trifolium Repens,
Substance Name: [2]
Agrimonia Eupatoria Flower; Ambrosia Artemisiifolia Whole; Anthoxanthum Odoratum Pollen; Arsenic Trioxide; Artemisia Abrotanum Flowering Top; Arundo Pliniana Root; Bambusa Bambos Stem; Cichorium Intybus Flower; Cynodon Dactylon Pollen; Dactylis Glomerata Top; Medicago Sativa Whole; Onion; Paspalum Notatum Pollen; Phleum Pratense Pollen; Poa Pratensis Pollen; Pulsatilla Pratensis Whole; Rumex Crispus Root; Schoenocaulon Officinale Seed; Secale Cereale Pollen; Sinapis Arvensis Flowering/fruiting Top; Sodium Chloride; Solidago Virgaurea Flowering Top; Sorghum Halepense Pollen; Strychnos Nux-vomica Seed; Taraxacum Officinale; Trifolium Pratense Flower; Trifolium Repens Flower; Wormwood; Wyethia Helenioides Root
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:
8a28f56a-6010-42e3-b360-e6e22b86222a
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-29-2020
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 44911-0547?

The NDC code 44911-0547 is assigned by the FDA to the product Weed Grass Antigens. It is commonly known by its generic name, allium cepa, arsenicum album, natrum muriaticum, nux vomica, pulsatilla (pratensis), abrotanum (artemisia abrotanum), absinthium, agrimonia eupatoria, flos, alfalfa, ambrosia artemisiaefolia, arundo mauritanica, bambusa arundinacea, cichorium intybus, flos, kentucky bluegrass, orchard grass, bermuda grass, johnson grass, rye grass, vernal grass, bahia grass, timothy grass, rumex crispus, sabadilla, sinapis arvensis, flos, solidago virgaurea, taraxacum officinale, trifolium pratense, trifolium repens, . 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: 44911-0547-1. 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 weed and grass allergies, such as hay fever and runny nose and sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with weed and grass allergies, such as hay fever and runny nose and sneezing.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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:

  • ONION (UNII: 492225Q21H)
  • ONION (UNII: 492225Q21H) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI)
  • PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (Active Moiety)
  • ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
  • ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (Active Moiety)
  • WORMWOOD (UNII: F84709P2XV)
  • WORMWOOD (UNII: F84709P2XV) (Active Moiety)
  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
  • MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)
  • ALFALFA (UNII: DJO934BRBD) (Active Moiety)
  • AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A)
  • AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (Active Moiety)
  • ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC)
  • ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (Active Moiety)
  • BAMBUSA BAMBOS STEM (UNII: NRA4497HC5)
  • BAMBUSA BAMBOS STEM (UNII: NRA4497HC5) (Active Moiety)
  • CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
  • CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
  • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
  • POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
  • DACTYLIS GLOMERATA TOP (UNII: J41552QKAK)
  • DACTYLIS GLOMERATA TOP (UNII: J41552QKAK) (Active Moiety)
  • CYNODON DACTYLON POLLEN (UNII: 175F461W10)
  • CYNODON DACTYLON WHOLE (UNII: 2Q8MR21NHK) (Active Moiety)
  • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
  • SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
  • SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O)
  • SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O) (Active Moiety)
  • ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y)
  • ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (Active Moiety)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
  • PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (Active Moiety)
  • PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
  • PHLEUM PRATENSE TOP (UNII: S7PW24BX20) (Active Moiety)
  • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
  • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
  • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO)
  • SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (Active Moiety)
  • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK)
  • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK) (Active Moiety)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
  • SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
  • TARAXACUM OFFICINALE (UNII: 39981FM375)
  • TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
  • TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
  • TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
  • TRIFOLIUM REPENS FLOWER (UNII: 49Y788T742)
  • TRIFOLIUM REPENS FLOWER (UNII: 49Y788T742) (Active Moiety)
  • WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N)
  • WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (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 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".