NDC 64578-0100 Hypothalmapath

  1. Labeler Index
  2. Energetix Corp
  3. NDC: 64578-0100 Hypothalmapath

NDC Product Code 64578-0100

NDC CODE: 64578-0100

Proprietary Name: Hypothalmapath 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: 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

  • 64578 - Energetix Corp

NDC 64578-0100-1

Package Description: 59.1 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Hypothalmapath with NDC 64578-0100 is a product labeled by Energetix Corp. The generic name of Hypothalmapath is . The product's dosage form is and is administered via form.

Labeler Name: Energetix Corp

Dosage Form: -

Product Type: 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.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)

Product Labeler Information

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

Labeler Name: Energetix Corp
Labeler Code: 64578
Start Marketing Date: 03-27-2014 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: 12-31-2017 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: I 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’.

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Hypothalmapath Product Label Images

Hypothalmapath 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

Gelsemium sempervirens 12X; Ginkgo biloba 6X; Glycyrrhiza glabra 4X; Hydrocotlye asiatica 4X; Hypothalamus 12X; Oleum santali 12X; Petroselinum sativum 4X; Pituitarum posterium 12X; Pyridoxinum hydrochloricum 12X; Senna 8X, 12X; Silicea 12X

* Please review the disclaimer below.