NDC 44911-0006 Dust Mix Antigens

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

NDC Product Code 44911-0006

NDC 44911-0006-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Dust Mix Antigens with NDC 44911-0006 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Dust Mix Antigens is barley, corn, house, mattress, millet, milo, oat, rice, rug, upholstery, wheat, arsenicum album, blatta orientalis, drosera, lycopodium clavatum, pothos foetidus, pulsatilla, . The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, Inc.

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.

Product Type: Human Otc Drug 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.

Dust Mix Antigens Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BARLEY 12 [hp_X]/mL
  • CORN 12 [hp_X]/mL
  • HOUSE DUST 12 [hp_X]/mL
  • MILLET 12 [hp_X]/mL
  • SORGHUM 12 [hp_X]/mL
  • OAT 12 [hp_X]/mL
  • BROWN RICE 12 [hp_X]/mL
  • WHEAT 12 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Energique, Inc.
Labeler Code: 44911
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 05-04-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 02-18-2024 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Dust Mix Antigens Product Label Images

Dust Mix Antigens Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

ACTIVE INGREDIENTS:  Barley 12X, 15X, 18X, 33X, Corn 12X, 15X, 18X, 33X, House 12X, 15X, 18X, 33X, Mattress 12X, 15X, 18X, 33X, Millet 12X, 15X, 18X, 33X, Milo 12X, 15X, 18X, 33X, Oat 12X, 15X, 18X, 33X, Rice 12X, 15X, 18X, 33X, Rug 12X, 15X, 18X, 33X, Upholstery 12X, 15X, 18X, 33X, Wheat 12X, 15X, 18X, 33X, Arsenicum album 12X, 15X, Blatta orientalis 12X, 15X, Drosera 12X, 15X, Lycopodium clavatum 12X, 15X, Pothos foetidus 12X, 15X, Pulsatilla 12X, 15X.

Otc - Purpose

INDICATIONS:  For temporary relief of allergies due to dust.


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 & 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.

Inactive Ingredient

INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.  In case of overdose, get medical help or contact a Poison Control Center right away.

Indications & Usage

INDICATIONS:  For temporary relief of allergies due to dust.

Otc - Questions

Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579800.869.8078

* Please review the disclaimer below.