NDC 44911-0043 Diabenex Hp

Aceticum Acidum, Colchicum Autumnale, Lacticum Acidum, Lycopodium Clavatum, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum, Uranium Nitricum

NDC Product Code 44911-0043

NDC CODE: 44911-0043

Proprietary Name: Diabenex Hp 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: Aceticum Acidum, Colchicum Autumnale, Lacticum Acidum, Lycopodium Clavatum, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum, Uranium Nitricum 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.

  • Acetic acid is used to treat an outer ear infection (external otitis). It works by stopping the growth of bacteria and fungus. Treating the infection reduces pain and swelling in the ear. Wetness in the ear canal can help bacteria and fungus to grow. This medication may also contain drying ingredients such as glycerin or alcohol. Drying of the ear canal helps to cure the infection.

NDC Code Structure

  • 44911 - Energique, Inc.

NDC 44911-0043-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Diabenex Hp with NDC 44911-0043 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Diabenex Hp is aceticum acidum, colchicum autumnale, lacticum acidum, lycopodium clavatum, phosphoricum acidum, phosphorus, syzygium jambolanum, uranium nitricum. 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.

Diabenex Hp 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.

  • ACETIC ACID 30 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 30 [hp_X]/mL
  • LACTIC ACID, DL- 30 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
  • PHOSPHORIC ACID 30 [hp_X]/mL
  • PHOSPHORUS 30 [hp_X]/mL
  • SYZYGIUM CUMINI SEED 30 [hp_X]/mL
  • URANYL NITRATE HEXAHYDRATE 30 [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: 10-05-2012 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.

Diabenex Hp Product Label Images

Diabenex Hp 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:

Aceticum Acidum 30X, Colchicum Autumnale 30X, Lacticum Acidum 30X, Lycopodium Clavatum 30X, Phosphoricum Acidum 30X, Phosphorus 30X, Syzygium Jambolanum 30X, Uranium Nitricum 30X.

Indications:

For temporary relief of symptoms of lethargy and fatigue in the afternoon after a meal, abnormal blood sugar.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms of lethargy and fatigue in the afternoon after a meal, abnormal blood sugar.****These statements are based upon traditional homeopathic practice. 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. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 20% Ethanol.

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.

Questions:

Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579   800-869-8078

Package Label Display:

ENERGIQUEsince 1987HOMEOPATHIC REMEDYDIABENEX HP1 fl. oz. (30 ml)

* Please review the disclaimer below.