NDC 64578-0060 Medi-chord

Homeopathic Liquid

NDC Product Code 64578-0060

NDC Product Information

Medi-chord with NDC 64578-0060 is a a human over the counter drug product labeled by Energetix Corporation. The generic name of Medi-chord is homeopathic liquid. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energetix Corporation

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.

Medi-chord 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 18 [hp_X]/59.1mL
  • ASPIRIN 18 [hp_X]/59.1mL
  • CORTICOTROPIN HUMAN 18 [hp_X]/59.1mL
  • ALUMINUM 18 [hp_X]/59.1mL
  • ATROPA BELLADONNA 12 [hp_X]/59.1mL
  • BENZENE 12 [hp_X]/59.1mL
  • CHLORAMPHENICOL 18 [hp_X]/59.1mL
  • CHLORPROMAZINE 18 [hp_X]/59.1mL
  • CORTISONE ACETATE 18 [hp_X]/59.1mL
  • ESTRONE 18 [hp_X]/59.1mL
  • SUS SCROFA ADRENAL GLAND 9 [hp_X]/59.1mL
  • GLYCYRRHIZA GLABRA 4 [hp_X]/59.1mL
  • PORK LIVER 9 [hp_X]/59.1mL
  • POTASSIUM IODIDE 12 [hp_X]/59.1mL
  • ARCTIUM LAPPA ROOT 4 [hp_X]/59.1mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/59.1mL
  • NITRIC ACID 12 [hp_X]/59.1mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/59.1mL
  • KEROSENE 18 [hp_X]/59.1mL
  • PHENACETIN 18 [hp_X]/59.1mL
  • PHOSPHORIC ACID 12 [hp_X]/59.1mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/59.1mL
  • LEAD 15 [hp_X]/59.1mL
  • FRANGULA PURSHIANA BARK 4 [hp_X]/59.1mL
  • PHENYL SALICYLATE 18 [hp_X]/59.1mL
  • SARSAPARILLA 4 [hp_X]/59.1mL
  • THYROID, UNSPECIFIED 9 [hp_X]/59.1mL
  • TRIFOLIUM PRATENSE FLOWER 4 [hp_X]/59.1mL
  • ELYMUS REPENS ROOT 4 [hp_X]/59.1mL

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)

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: Energetix Corporation
Labeler Code: 64578
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: 09-21-2017 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.

Medi-chord Product Label Images

Medi-chord 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

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

* Please review the disclaimer below.

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