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,

Energique, Inc.
Human Otc Drug
NDC 44911-0547

Weed Grass Antigens also known as 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 human otc drug labeled by 'Energique, Inc.'. National Drug Code (NDC) number for Weed Grass Antigens is 44911-0547. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Weed Grass Antigens drug includes Agrimonia Eupatoria Flower - 16 [hp_X]/mL Ambrosia Artemisiifolia Whole - 16 [hp_X]/mL Anthoxanthum Odoratum Pollen - 16 [hp_X]/mL Arsenic Trioxide - 12 [hp_X]/mL Artemisia Abrotanum Flowering Top - 16 [hp_X]/mL Arundo Pliniana Root - 16 [hp_X]/mL Bambusa Bambos Stem - 16 [hp_X]/mL Cichorium Intybus Flower - 16 [hp_X]/mL Cynodon Dactylon Pollen - 16 [hp_X]/mL Dactylis Glomerata Top - 16 [hp_X]/mL and more. The currest status of Weed Grass Antigens drug is Active.

Drug Information:

Drug NDC:	44911-0547
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Weed Grass Antigens
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary 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,
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Energique, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	AGRIMONIA EUPATORIA FLOWER - 16 [hp_X]/mL AMBROSIA ARTEMISIIFOLIA WHOLE - 16 [hp_X]/mL ANTHOXANTHUM ODORATUM POLLEN - 16 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL ARTEMISIA ABROTANUM FLOWERING TOP - 16 [hp_X]/mL ARUNDO PLINIANA ROOT - 16 [hp_X]/mL BAMBUSA BAMBOS STEM - 16 [hp_X]/mL CICHORIUM INTYBUS FLOWER - 16 [hp_X]/mL CYNODON DACTYLON POLLEN - 16 [hp_X]/mL DACTYLIS GLOMERATA TOP - 16 [hp_X]/mL Load more... MEDICAGO SATIVA WHOLE - 16 [hp_X]/mL ONION - 12 [hp_X]/mL PASPALUM NOTATUM POLLEN - 16 [hp_X]/mL PHLEUM PRATENSE POLLEN - 16 [hp_X]/mL POA PRATENSIS POLLEN - 16 [hp_X]/mL PULSATILLA PRATENSIS WHOLE - 12 [hp_X]/mL RUMEX CRISPUS ROOT - 16 [hp_X]/mL SCHOENOCAULON OFFICINALE SEED - 16 [hp_X]/mL SECALE CEREALE POLLEN - 16 [hp_X]/mL SINAPIS ARVENSIS FLOWERING/FRUITING TOP - 16 [hp_X]/mL SODIUM CHLORIDE - 12 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP - 16 [hp_X]/mL SORGHUM HALEPENSE POLLEN - 16 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL TARAXACUM OFFICINALE - 16 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER - 16 [hp_X]/mL TRIFOLIUM REPENS FLOWER - 16 [hp_X]/mL WORMWOOD - 16 [hp_X]/mL WYETHIA HELENIOIDES ROOT - 16 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	29 May, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	10 May, 2026
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Energique, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	0363113701661
UPC stands for Universal Product Code.
NUI:	N0000185006 N0000175629 N0000184306 N0000185001 M0017130 M0000728 N0000185371 M0006342 M0022575 N0000185367 N0000185375 M0016962 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	5811MI029U 9W34L2CQ9A 2KIK19R45Y S7V92P67HO QG07G580U0 ZXE7LB03WC NRA4497HC5 HW54500A89 175F461W10 J41552QKAK Load more... DJO934BRBD 492225Q21H V003SHB7VK 65M88RW2EG SCB8J7LS3T 8E272251DI 9N1RM2S62C 6NAF1689IO I6KAZ8AO1O WWX61E1ZAK 451W47IQ8X 5405K23S50 577VA5B4HP 269XH13919 39981FM375 4JS0838828 49Y788T742 F84709P2XV J10PD1AQ0N
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Pollen Allergenic Extract [EPC] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Pollen Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Pollen [CS] Allergens [CS] Dietary Proteins [CS] Vegetable Proteins [CS] Plant Proteins [CS] Seed Storage Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Non-Standardized Pollen Allergenic Extract [EPC] Plant Proteins [CS] Pollen [CS] Seed Storage Proteins [CS] Standardized Pollen Allergenic Extract [EPC] Vegetable Proteins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
44911-0547-1	30 mL in 1 BOTTLE, DROPPER (44911-0547-1)	01 Jun, 2020	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Weed Grass Antigens

Allium Cepa & more..

Liquid
Energique, Inc.
NDC: 44911-0553

Weed Grass Antigens

Allium Cepa & more..

Liquid
Energique, Inc.
NDC: 44911-0547

Purpose:

Indications: may temporarily relieve symptoms associated with weed and grass pollens, such as runny nose, sneezing, and itchy, watery eyes.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

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, onion onion arsenic trioxide arsenic cation (3+) sodium chloride chloride ion strychnos nux-vomica seed strychnos nux-vomica seed pulsatilla pratensis whole pulsatilla pratensis whole artemisia abrotanum flowering top artemisia abrotanum flowering top wormwood wormwood agrimonia eupatoria flower agrimonia eupatoria flower medicago sativa whole alfalfa ambrosia artemisiifolia whole ambrosia artemisiifolia arundo pliniana root arundo pliniana root bambusa bambos stem bambusa bambos stem cichorium intybus flower cichorium intybus flower poa pratensis pollen poa pratensis pollen dactylis glomerata top dactylis glomerata top cynodon dactylon pollen cynodon dactylon whole sorghum halepense pollen sorghum halepense pollen secale cereale pollen secale cereale pollen anthoxanthum odoratum pollen anthoxanthum odoratum pollen paspalum notatum pollen paspalum notatum pollen phleum pratense pollen phleum pratense top rumex crispus root rumex crispus root schoenocaulon officinale seed schoenocaulon officinale seed sinapis arvensis flowering/fruiting top sinapis arvensis flowering/fruiting top solidago virgaurea flowering top solidago virgaurea flowering top taraxacum officinale taraxacum officinale trifolium pratense flower trifolium pratense flower trifolium repens flower trifolium repens flower wyethia helenioides root wyethia helenioides root water alcohol

Indications and Usage:

Warnings:

Warnings: if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. do not use if tamper evident seal is broken or missing. store in a cool, dry place.

Dosage and Administration:

Directions: adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. if symptoms persist for more than 7 days, consult your health care professional. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: energique since 1987 homeopathic remedy weed/grass antigens 1 fl. oz. (30 ml) weed grass antigens

Further Questions:

Questions: dist. by energique, inc. 201 apple blvd. woodbine, ia 51579 800.869.8078

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.