NDC 44911-0547 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,

NDC Product Code 44911-0547

NDC CODE: 44911-0547

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, 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, 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).
  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.

NDC Code Structure

  • 44911 - Energique, Inc.

NDC 44911-0547-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Weed Grass Antigens with NDC 44911-0547 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, 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, . 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
  • SODIUM CHLORIDE 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL
  • ARTEMISIA ABROTANUM FLOWERING TOP 16 [hp_X]/mL
  • WORMWOOD 16 [hp_X]/mL
  • AGRIMONIA EUPATORIA FLOWER 16 [hp_X]/mL
  • MEDICAGO SATIVA WHOLE 16 [hp_X]/mL
  • AMBROSIA ARTEMISIIFOLIA WHOLE 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
  • POA PRATENSIS POLLEN 16 [hp_X]/mL
  • DACTYLIS GLOMERATA TOP 16 [hp_X]/mL
  • CYNODON DACTYLON POLLEN 16 [hp_X]/mL
  • SORGHUM HALEPENSE POLLEN 16 [hp_X]/mL
  • SECALE CEREALE POLLEN 16 [hp_X]/mL
  • ANTHOXANTHUM ODORATUM POLLEN 16 [hp_X]/mL
  • PASPALUM NOTATUM POLLEN 16 [hp_X]/mL
  • PHLEUM PRATENSE POLLEN 16 [hp_X]/mL
  • RUMEX CRISPUS ROOT 16 [hp_X]/mL
  • SCHOENOCAULON OFFICINALE SEED 16 [hp_X]/mL
  • SINAPIS ARVENSIS FLOWERING/FRUITING TOP 16 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 16 [hp_X]/mL
  • TARAXACUM OFFICINALE 16 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 16 [hp_X]/mL
  • TRIFOLIUM REPENS FLOWER 16 [hp_X]/mL
  • WYETHIA HELENIOIDES ROOT 16 [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: 05-29-2020 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: 12-31-2021 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 Label Images

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:

(in each drop): 8.33% of Allium Cepa 12X, 15X, Arsenicum Album 12X, 15X, Natrum Muriaticum 12X, 15X, Nux Vomica 12X, 15X, Pulsatilla (Pratensis) 12X, 15X. 2.78% of Kentucky Bluegrass 16X, 24X, 30X, Orchard Grass 16X, 24X, 30X, Bermuda Grass 16X, 24X, 30X, Johnson Grass 16X, 24X, 30X, Rye Grass 16X, 24X, 30X, Vernal Grass 16X, 24X, 30X, Bahia Grass 16X, 24X, 30X, Timothy Grass 16X, 24X, 30X. 0.017% of Abrotanum (Artemisia Abrotanum) 16X, 24X, 30X, Absinthium 16X, 24X, 30X, Agrimonia Eupatoria, Flos 16X, 24X, 30X, Alfalfa 16X, 24X, 30X, Ambrosia Artemisiaefolia 16X, 24X, 30X, Arundo Mauritanica 16X, 24X, 30X, Bambusa Arundinacea 16X, 24X, 30X, Cichorium Intybus, Flos 16X, 24X, 30X, Rumex Crispus 16X, 24X, 30X, Sabadilla 16X, 24X, 30X, Sinapis Arvensis, Flos 16X, 24X, 30X, Solidago Virgaurea 16X, 24X, 30X, Taraxacum Officinale 16X, 24X, 30X, Trifolium Pratense 16X, 24X, 30X, Trifolium Repens 16X, 24X, 30X, Wyethia Helenioides 16X, 24X, 30X.

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.

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:

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.

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.

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.

Inactive Ingredients:

Demineralized water, 20% Ethanol.

Questions:

Dist. by Energique, Inc.201 Apple Blvd.Woodbine, IA 51579800-869-8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYWEED/GRASSANTIGENS1 fl. oz. (30 ml)

* Please review the disclaimer below.