NDC 57293-4416 Constipation

Aluminum, Phenol, Chelidonium Majus, Graphite, Potassium Carbonate, Veronicastrum Virginicum Root, Magnesium Chloride, Mercurius Solubilis

NDC Product Code 57293-4416

NDC Code: 57293-4416

Proprietary Name: Constipation 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: Aluminum, Phenol, Chelidonium Majus, Graphite, Potassium Carbonate, Veronicastrum Virginicum Root, Magnesium Chloride, Mercurius Solubilis 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

  • 57293 - Bioenergetics, Inc.
    • 57293-4416 - Constipation

NDC 57293-4416-2

Package Description: 60 mL in 1 BOTTLE, GLASS

NDC Product Information

Constipation with NDC 57293-4416 is a a human over the counter drug product labeled by Bioenergetics, Inc.. The generic name of Constipation is aluminum, phenol, chelidonium majus, graphite, potassium carbonate, veronicastrum virginicum root, magnesium chloride, mercurius solubilis. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioenergetics, 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.

Constipation 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.

  • ALUMINUM 30 [hp_X]/60mL
  • PHENOL 12 [hp_X]/60mL
  • GRAPHITE 12 [hp_X]/60mL

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.

Product Labeler Information

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

Labeler Name: Bioenergetics, Inc.
Labeler Code: 57293
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: 07-12-1991 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: 12-31-2019 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.

Constipation Product Label Images

Constipation 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

Aluminum met 30x,Carbolic acid 12x,Chelidonium maj 6x,Graphites 12x, Kali carb 12x,Leptandra virg 6x,Magnesia mur 12x,Mercurius Sol 12x

Inactive Ingredients:

Alcohol 20%, purified water.


In general, 10 drops under the tongue 3 times daily. In acute conditions, 10 drops every 15 minutes. 

Children, one half the above dosage. For children 2 years and under, and for people nursing a baby or pregnant, seek the advice of a health professional before use.

Do Not Use


* Please review the disclaimer below.

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