Dust Mix Antigens

Barley, Corn, House, Mattress, Millet, Milo, Oat, Rice, Rug, Upholstery, Wheat, Arsenicum Album, Blatta Orientalis, Drosera, Lycopodium Clavatum, Pothos Foetidus, Pulsatilla,

Energique, Inc.
Human Otc Drug
NDC 44911-0006

Dust Mix Antigens also known as Barley, Corn, House, Mattress, Millet, Milo, Oat, Rice, Rug, Upholstery, Wheat, Arsenicum Album, Blatta Orientalis, Drosera, Lycopodium Clavatum, Pothos Foetidus, Pulsatilla, is a human otc drug labeled by 'Energique, Inc.'. National Drug Code (NDC) number for Dust Mix Antigens is 44911-0006. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Dust Mix Antigens drug includes Anemone Pulsatilla - 12 [hp_X]/mL Arsenic Trioxide - 12 [hp_X]/mL Barley - 12 [hp_X]/mL Blatta Orientalis - 12 [hp_X]/mL Brown Rice - 12 [hp_X]/mL Corn - 12 [hp_X]/mL Drosera Rotundifolia - 12 [hp_X]/mL House Dust - 12 [hp_X]/mL Lycopodium Clavatum Spore - 12 [hp_X]/mL Millet - 12 [hp_X]/mL and more. The currest status of Dust Mix Antigens drug is Active.

Drug Information:

Drug NDC:	44911-0006
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:	Dust Mix 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:	Barley, Corn, House, Mattress, Millet, Milo, Oat, Rice, Rug, Upholstery, Wheat, Arsenicum Album, Blatta Orientalis, Drosera, Lycopodium Clavatum, Pothos Foetidus, Pulsatilla,
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:	ANEMONE PULSATILLA - 12 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL BARLEY - 12 [hp_X]/mL BLATTA ORIENTALIS - 12 [hp_X]/mL BROWN RICE - 12 [hp_X]/mL CORN - 12 [hp_X]/mL DROSERA ROTUNDIFOLIA - 12 [hp_X]/mL HOUSE DUST - 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/mL MILLET - 12 [hp_X]/mL Load more... OAT - 12 [hp_X]/mL SORGHUM - 12 [hp_X]/mL SYMPLOCARPUS FOETIDUS ROOT - 12 [hp_X]/mL WHEAT - 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:	04 May, 2012
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	18 Feb, 2024
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:	20 Jun, 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:	N0000185371 N0000175629 N0000184306 M0000728 M0006342 N0000185016 N0000185365 N0000185001 M0028968 N0000185374 M0006896
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	I76KB35JEV S7V92P67HO 5PWM7YLI7R 535787266D 659G217HPG 0N8672707O QR44N9XPJQ EYO007VX98 C88X29Y479 TJR6B3R47P Load more... Z6J799EAJK CUL9PN8ELJ R88254608W 4J2I0SN84Y
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 Food Allergenic Extract [EPC] Non-Standardized Insect Allergenic Extract [EPC] Non-Standardized House Dust 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:	Allergens [CS] Dietary Proteins [CS] Insect Proteins [CS] House Dust [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] Grain Proteins [EXT] House Dust [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Insect Proteins [CS] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized House Dust Allergenic Extract [EPC] Non-Standardized Insect Allergenic Extract [EPC]
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
44911-0006-1	30 mL in 1 BOTTLE, DROPPER (44911-0006-1)	04 May, 2012	18 Feb, 2024	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

Dust Mix Antigens

Barley & more..

Liquid
Energique, Inc.
NDC: 44911-0006

Purpose:

Indications: may temporarily relieve symptoms associated with dust allergies.** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Dust mix antigens barley, corn, house, mattress, millet, milo, oat, rice, rug, upholstery, wheat, arsenicum album, blatta orientalis, drosera, lycopodium clavatum, pothos foetidus, pulsatilla, barley barley corn corn house dust house dust millet millet sorghum sorghum oat oat brown rice brown rice wheat wheat arsenic trioxide arsenic cation (3+) blatta orientalis blatta orientalis lycopodium clavatum spore lycopodium clavatum spore symplocarpus foetidus root symplocarpus foetidus root anemone pulsatilla anemone pulsatilla drosera rotundifolia drosera rotundifolia alcohol water

Indications and Usage:

Indications: may temporarily relieve symptoms associated with dust allergies.** **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 dust mix antigens 1 fl. oz. (30 ml) dust mix 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.