NDC 57293-4402 Stress Release

Aconitum Napellus, Atropa Belladonna, Saffron, Strychnos Ignatii Seed, Dibasic Potassium Phosphate, Strychnos Nux-vomica Seed, Valerian

NDC Product Code 57293-4402

NDC CODE: 57293-4402

Proprietary Name: Stress Release 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: Aconitum Napellus, Atropa Belladonna, Saffron, Strychnos Ignatii Seed, Dibasic Potassium Phosphate, Strychnos Nux-vomica Seed, Valerian 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.

NDC 57293-4402-2

Package Description: 60 mL in 1 BOTTLE, GLASS

NDC Product Information

Stress Release with NDC 57293-4402 is a a human over the counter drug product labeled by Bioenergetics, Inc.. The generic name of Stress Release is aconitum napellus, atropa belladonna, saffron, strychnos ignatii seed, dibasic potassium phosphate, strychnos nux-vomica seed, valerian. The product's dosage form is liquid and is administered via oral form.

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.

Stress Release 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.


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: 01-28-1989 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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Stress Release Product Label Images

Stress Release 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

Aconitum napellus 12x, Belladonna 12x, Croscus sat 9x, Ignatia amara 6x, Kali phos 12x, Nux vomica 12x, Valeriana off 6x

Inactive Ingredients:

Alcohol 20%, purified water.

Dosage:

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

IF BioE IMPRINTED SEAL ON NECK IS BROKEN

* Please review the disclaimer below.