Weed Grass Antigens

Allium Cepa, Arsenicum Album, Nux Vomica, Pulsatilla (vulgaris), Agrimonia Eupatoria, Alfalfa, Amaranthus (carelessweed), Artemisia Vulgaris, Bamboo (leaf), Kentucky Blue, Lambs Quarter, Marsh Elder (combination), Meadow Fescue, Orchard, Perennial Rye, Redtop, Rough Pigweed, Rumex/sorrel (combination), Sagebrush, Solidago Virguarea, Spiny Pigweed, Sweet Vernal, Taraxacum Officinale, Timothy, Trifolium Pratense, Trifolium Repens, Western Ragweed

Energique, Inc.
Human Otc Drug
NDC 44911-0032

Weed Grass Antigens also known as Allium Cepa, Arsenicum Album, Nux Vomica, Pulsatilla (vulgaris), Agrimonia Eupatoria, Alfalfa, Amaranthus (carelessweed), Artemisia Vulgaris, Bamboo (leaf), Kentucky Blue, Lambs Quarter, Marsh Elder (combination), Meadow Fescue, Orchard, Perennial Rye, Redtop, Rough Pigweed, Rumex/sorrel (combination), Sagebrush, Solidago Virguarea, Spiny Pigweed, Sweet Vernal, Taraxacum Officinale, Timothy, Trifolium Pratense, Trifolium Repens, Western Ragweed is a human otc drug labeled by 'Energique, Inc.'. National Drug Code (NDC) number for Weed Grass Antigens is 44911-0032. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Weed Grass Antigens drug includes Agrostis Stolonifera Pollen - 12 [hp_X]/mL Alfalfa - 12 [hp_X]/mL Amaranthus Hybridus Pollen - 12 [hp_X]/mL Amaranthus Retroflexus Pollen - 12 [hp_X]/mL Amaranthus Spinosus Pollen - 12 [hp_X]/mL Ambrosia Psilostachya Pollen - 12 [hp_X]/mL Anemone Pulsatilla - 12 [hp_X]/mL Anthoxanthum Odoratum Pollen - 12 [hp_X]/mL Arsenic Trioxide - 12 [hp_X]/mL Artemisia Tridentata Pollen - 12 [hp_X]/mL and more. The currest status of Weed Grass Antigens drug is Active.

Drug Information:

Drug NDC:	44911-0032
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, Nux Vomica, Pulsatilla (vulgaris), Agrimonia Eupatoria, Alfalfa, Amaranthus (carelessweed), Artemisia Vulgaris, Bamboo (leaf), Kentucky Blue, Lambs Quarter, Marsh Elder (combination), Meadow Fescue, Orchard, Perennial Rye, Redtop, Rough Pigweed, Rumex/sorrel (combination), Sagebrush, Solidago Virguarea, Spiny Pigweed, Sweet Vernal, Taraxacum Officinale, Timothy, Trifolium Pratense, Trifolium Repens, Western Ragweed
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:	AGROSTIS STOLONIFERA POLLEN - 12 [hp_X]/mL ALFALFA - 12 [hp_X]/mL AMARANTHUS HYBRIDUS POLLEN - 12 [hp_X]/mL AMARANTHUS RETROFLEXUS POLLEN - 12 [hp_X]/mL AMARANTHUS SPINOSUS POLLEN - 12 [hp_X]/mL AMBROSIA PSILOSTACHYA POLLEN - 12 [hp_X]/mL ANEMONE PULSATILLA - 12 [hp_X]/mL ANTHOXANTHUM ODORATUM POLLEN - 12 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL ARTEMISIA TRIDENTATA POLLEN - 12 [hp_X]/mL Load more... ARTEMISIA VULGARIS POLLEN - 12 [hp_X]/mL BAMBUSA VULGARIS LEAF - 12 [hp_X]/mL CHENOPODIUM ALBUM POLLEN - 12 [hp_X]/mL DACTYLIS GLOMERATA POLLEN - 12 [hp_X]/mL FESTUCA PRATENSIS POLLEN - 12 [hp_X]/mL IVA ANGUSTIFOLIA POLLEN - 12 [hp_X]/mL IVA ANNUA POLLEN - 12 [hp_X]/mL LOLIUM PERENNE POLLEN - 12 [hp_X]/mL ONION - 12 [hp_X]/mL PHLEUM PRATENSE POLLEN - 12 [hp_X]/mL POA PRATENSIS TOP - 12 [hp_X]/mL RUMEX ACETOSA WHOLE - 12 [hp_X]/mL RUMEX CRISPUS TOP - 12 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP - 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL TARAXACUM OFFICINALE - 12 [hp_X]/mL TRIFOLIUM PRATENSE POLLEN - 12 [hp_X]/mL TRIFOLIUM REPENS POLLEN - 12 [hp_X]/mL XANTHIUM STRUMARIUM POLLEN - 12 [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:	08 Oct, 2012
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	15 Aug, 2023
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:	09 May, 2026
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.
NUI:	N0000185367 N0000175629 N0000184306 N0000185001 M0017130 M0000728 N0000185006 N0000185371 M0006342 M0022575 N0000185375 M0016962 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	255H8VT4RK DJO934BRBD EK7F0414PI 73B14PX5FW 380W4HYR6N RX18M46K8L I76KB35JEV 2KIK19R45Y S7V92P67HO YI19RB8YFD Load more... ANT994T71D EMY54R518C 098LKX5NCN 83N78IDA7P A0WFQ8P6N1 UBW6O1H50I Y2U5S5PF22 4T81LB52R0 492225Q21H 65M88RW2EG 7EA48700V9 IA49H9SY8T S9T422Q956 5405K23S50 269XH13919 39981FM375 3SNK70F46Y IQV1MZ32RL 2QOF601J1M
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:	Non-Standardized Pollen Allergenic Extract [EPC] Standardized Pollen Allergenic Extract [EPC] Non-Standardized Food 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
44911-0032-1	60 mL in 1 BOTTLE, DROPPER (44911-0032-1)	08 Oct, 2012	15 Aug, 2023	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: 44911-0032

Purpose:

Indications: 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.

Product Elements:

Weed grass antigens allium cepa, arsenicum album, nux vomica, pulsatilla (vulgaris), agrimonia eupatoria, alfalfa, amaranthus (carelessweed), artemisia vulgaris, bamboo (leaf), kentucky blue, lambs quarter, marsh elder (combination), meadow fescue, orchard, perennial rye, redtop, rough pigweed, rumex/sorrel (combination), sagebrush, solidago virguarea, spiny pigweed, sweet vernal, taraxacum officinale, timothy, trifolium pratense, trifolium repens, western ragweed onion onion arsenic trioxide arsenic cation (3+) strychnos nux-vomica seed strychnos nux-vomica seed anemone pulsatilla anemone pulsatilla alfalfa alfalfa amaranthus hybridus pollen amaranthus hybridus pollen bambusa vulgaris leaf bambusa vulgaris leaf xanthium strumarium pollen xanthium strumarium pollen taraxacum officinale taraxacum officinale solidago virgaurea flowering top solidago virgaurea flowering top poa pratensis top poa pratensis top chenopodium album pollen chenopodium album pollen iva angustifolia pollen iva angustifolia pollen iva annua pollen iva annua pollen festuca pratensis pollen festuca pratensis pollen artemisia vulgaris pollen artemisia vulgaris pollen dactylis glomerata pollen dactylis glomerata pollen lolium perenne pollen lolium perenne pollen trifolium pratense pollen trifolium pratense pollen agrostis stolonifera pollen agrostis stolonifera pollen amaranthus retroflexus pollen amaranthus retroflexus pollen artemisia tridentata pollen artemisia tridentata pollen amaranthus spinosus pollen amaranthus spinosus pollen anthoxanthum odoratum pollen anthoxanthum odoratum pollen phleum pratense pollen phleum pratense pollen ambrosia psilostachya pollen ambrosia psilostachya pollen trifolium repens pollen trifolium repens pollen rumex crispus top rumex crispus top rumex acetosa whole rumex acetosa whole water alcohol

Indications and Usage:

Indications: 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.

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, 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 2 fl. oz. (60 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.