NDC 64578-0100 Hypothalmapath

Product Information

What is NDC 64578-0100?

The NDC code 64578-0100 is assigned by the FDA to the product Hypothalmapath which is product labeled by Energetix Corp. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 64578-0100-1 59.1 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code64578-0100
Proprietary Name 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.
Hypothalmapath
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Energetix Corp
Labeler Code64578
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
03-27-2014
Listing Expiration Date 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.
12-31-2017
Exclude Flag 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".
I
NDC Code Structure

Product Packages

NDC Code 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.

Product Details

Hypothalmapath Active Ingredients UNII Codes

Hypothalmapath Inactive Ingredients UNII Codes

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.

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Hypothalmapath Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



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.