NDC 44911-0032 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

NDC Product Code 44911-0032

NDC CODE: 44911-0032

Proprietary Name: Weed Grass Antigens What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).

NDC Code Structure

  • 44911 - Energique, Inc.

NDC 44911-0032-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Weed Grass Antigens with NDC 44911-0032 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Weed Grass Antigens is 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. 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.

Weed Grass 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.

  • ONION 12 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • ANEMONE PULSATILLA 12 [hp_X]/mL
  • ALFALFA 12 [hp_X]/mL
  • AMARANTHUS HYBRIDUS POLLEN 12 [hp_X]/mL
  • BAMBUSA VULGARIS LEAF 12 [hp_X]/mL
  • XANTHIUM STRUMARIUM POLLEN 12 [hp_X]/mL
  • TARAXACUM OFFICINALE 12 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]/mL
  • POA PRATENSIS TOP 12 [hp_X]/mL
  • CHENOPODIUM ALBUM POLLEN 12 [hp_X]/mL
  • IVA ANGUSTIFOLIA POLLEN 12 [hp_X]/mL
  • IVA ANNUA POLLEN 12 [hp_X]/mL
  • FESTUCA PRATENSIS POLLEN 12 [hp_X]/mL
  • ARTEMISIA VULGARIS POLLEN 12 [hp_X]/mL
  • DACTYLIS GLOMERATA POLLEN 12 [hp_X]/mL
  • LOLIUM PERENNE POLLEN 12 [hp_X]/mL
  • TRIFOLIUM PRATENSE POLLEN 12 [hp_X]/mL
  • AGROSTIS STOLONIFERA POLLEN 12 [hp_X]/mL
  • AMARANTHUS RETROFLEXUS POLLEN 12 [hp_X]/mL
  • ARTEMISIA TRIDENTATA POLLEN 12 [hp_X]/mL
  • AMARANTHUS SPINOSUS POLLEN 12 [hp_X]/mL
  • ANTHOXANTHUM ODORATUM POLLEN 12 [hp_X]/mL
  • PHLEUM PRATENSE POLLEN 12 [hp_X]/mL
  • AMBROSIA PSILOSTACHYA POLLEN 12 [hp_X]/mL
  • TRIFOLIUM REPENS POLLEN 12 [hp_X]/mL
  • RUMEX CRISPUS TOP 12 [hp_X]/mL
  • RUMEX ACETOSA WHOLE 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.

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

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: 10-08-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

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.

Weed Grass 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

Active Ingredients:

Allium cepa 12X, 15X, Arsenicum album 12X, 15X, Nux vomica 12X, 15X, Pulsatilla 12X, 15X, Alfalfa 12X, 15X, 18X, 33X, Amaranthus (Careless weed) 12X, 15X, 18X, 33X, Bamboo 12X, 15X, 18X, 33X, Cocklebur 12X, 15X, 18X, 33X, Dandelion 12X, 15X, 18X, 33X, Goldenrod 12X, 15X, 18X, 33X, Kentucky blue 12X, 15X, 18X, 33X, Lambs quarter 12X, 15X, 18X, 33X, Marsh Elder narrow leaf 12X. 15X, 18X, 33X, Marsh Elder rough 12X, 15X, 18X, 33X, Meadow fescue 12X, 15X, 18X, 33X, Mugwort 12X, 15X, 18X, 33X, Orchard 12X, 15X, 18X, 33X, Perennial rye 12X, 15X, 18X, 33X, Red clover 12X, 15X, 18X, 33X, Redtop 12X 15X, 18X, 33X, Rough pigweed 12X, 15X, 18X, 33X, Sagebrush 12X, 15X, 18X, 33X, Spiny pigweed 12X, 15X, 18X, 33X, Sweet vernal 12X, 15X, 18X, 33X, Timothy 12X, 15X, 18X, 33X, Western ragweed 12X, 15X, 18X, 33X, White clover 12X, 15X, 18X, 33X, Yellow dock 12X, 15X, 18X, 33X, Sorrel 12X, 15X, 18X, 33X.

Indications:

For temporary relief of allergies due to weeds and grasses.**** These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For temporary relief of allergies due to weeds and grasses.**** These statements are based upon traditional homeopathic practic e. They have not been reviewed by the Food and Drug Administration.

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.

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. Consule a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineraliaed water, 20% Ethanol.

Keep Out Of Reach Of Children:

In case of overdose, get medical help or contact a Poison Control Center right away.

Otc - Questions

Dist. byEnergique, Inc.201 Apple Blvd.Woodbine, IA 51579800.869.8078

Package Label Display

ENERGIQUEHOMEOPATHIC REMEDYWEED GRASS ANTIGENS2 fl oz. (60 ml)

* Please review the disclaimer below.