NDC 44911-0355 Allerphenex II

Acetylcholine Chloride, Acetaldehyde, Adrenalinum, Caffeic Acid, Candida Albicans, Chlorogenic Acid, Cinnamic Acid, Coumarinum, Cysteinum, Gallicum Acidum, Hepar Suis, Histaminum Hydrochloricum, Indolum, Malvin, Mannan, Menadione, Norepinephrine, Octopamine (hydrochloride), Pancreas Suis, Phenyl Isothiocyanate, Phloridzinum, Quercetin, Salsolinol, Serotonin (hydrochloride)

NDC Product Code 44911-0355

NDC Code: 44911-0355

Proprietary Name: Allerphenex II 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: Acetylcholine Chloride, Acetaldehyde, Adrenalinum, Caffeic Acid, Candida Albicans, Chlorogenic Acid, Cinnamic Acid, Coumarinum, Cysteinum, Gallicum Acidum, Hepar Suis, Histaminum Hydrochloricum, Indolum, Malvin, Mannan, Menadione, Norepinephrine, Octopamine (hydrochloride), Pancreas Suis, Phenyl Isothiocyanate, Phloridzinum, Quercetin, Salsolinol, Serotonin (hydrochloride) 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.

NDC Code Structure

  • 44911 - Energique, Inc.

NDC 44911-0355-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Allerphenex II with NDC 44911-0355 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Allerphenex II is acetylcholine chloride, acetaldehyde, adrenalinum, caffeic acid, candida albicans, chlorogenic acid, cinnamic acid, coumarinum, cysteinum, gallicum acidum, hepar suis, histaminum hydrochloricum, indolum, malvin, mannan, menadione, norepinephrine, octopamine (hydrochloride), pancreas suis, phenyl isothiocyanate, phloridzinum, quercetin, salsolinol, serotonin (hydrochloride). 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.

Allerphenex II 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.

  • ACETYLCHOLINE CHLORIDE 200 [hp_X]/mL
  • ACETALDEHYDE 200 [hp_X]/mL
  • EPINEPHRINE 200 [hp_X]/mL
  • CAFFEIC ACID 200 [hp_X]/mL
  • CANDIDA ALBICANS 200 [hp_X]/mL
  • CHLOROGENIC ACID 200 [hp_X]/mL
  • CINNAMIC ACID 200 [hp_X]/mL
  • COUMARIN 200 [hp_X]/mL
  • CYSTEINE 200 [hp_X]/mL
  • GALLIC ACID MONOHYDRATE 200 [hp_X]/mL
  • PORK LIVER 200 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 200 [hp_X]/mL
  • INDOLE 200 [hp_X]/mL
  • MALVIN 200 [hp_X]/mL
  • YEAST MANNAN 200 [hp_X]/mL
  • MENADIONE 200 [hp_X]/mL
  • NOREPINEPHRINE 200 [hp_X]/mL
  • OCTOPAMINE HYDROCHLORIDE 200 [hp_X]/mL
  • SUS SCROFA PANCREAS 200 [hp_X]/mL
  • PHENYL ISOTHIOCYANATE 200 [hp_X]/mL
  • PHLORIZIN 200 [hp_X]/mL
  • QUERCETIN 200 [hp_X]/mL
  • SALSOLINOL HYDROCHLORIDE 200 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 200 [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.

  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • WATER (UNII: 059QF0KO0R)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

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.

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: 04-20-2016 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.

Allerphenex II Product Label Images

Allerphenex II 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:

Acetylcholine Chloride 200X, 400X, 800X, 1000X, Acetaldehyde 200X, 400X, 800X, 1000X, Adrenalinum 200X, 400X, 800X, 1000X, Caffeic Acid 200X, 400X, 800X, 1000X, Candida Albicans 12X, 30X, 60X, 100X, Chlorogenic Acid 200X, 400X, 800X, 1000X, Cinnamic Acid 200X, 400X, 800X, 1000X, Coumarinum 200X, 400X, 800X, 1000X, Cysteinum 200X, 400X, 800X, 1000X, Gallicum Acidum 200X, 400X, 800X, 1000X, Hepar Suis 200X, 400X, 800X, 1000X, Histaminum Hydrochloricum 200X, 400X, 800X, 1000X, Indolum 200X, 400X, 800X, 1000X, Malvin 200X, 400X, 800X, 1000X, Mannan 200X, 400X, 800X, 1000X, Menadione 200X, 400X, 800X, 1000X, Norepinephrine 200X, 400X, 800X, 1000X, Octopamine (Hydrochloride) 200X, 400X, 800X, 1000X, Pancreas Suis 200X, 400X, 800X, 1000X, Phenyl Isothiocyanate 200X, 400X, 800X, 1000X, Phloridzinum 200X, 400X, 800X, 1000X, Quercetin 200X, 400X, 800X, 1000X, Salsolinol 200X, 400X, 800X, 1000X, Serotonin (Hydrochloride) 200X, 400X, 800X, 1000X.

Indications:

Phenolic sensitivity.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Phenolic sensitivity.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breastfeeding, 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, consult your health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Citric Acid, Demineralized water, Potassium Sorbate.

Questions:

Dist. by Energique, Inc.201 Apple Blvd.Woodbine, IA 51579800.868.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYALLERPHENEX II1 fl. oz. (30 ml)

* Please review the disclaimer below.