NDC 64578-0151 Tox-chord

Alfalfa, Alumina, Benzoicum Ac, Carboneum, Cetraria, Folliculinum, Fucus, Fumaricum Ac, Hepar Suis, Kali Carb, Kreosotum, Nat Mur, Paraffinum, Petroleum, Phosphoricum Ac, Phos, Pix Liquida, Plantago, Plumb Met, Pulsatilla, Radium Brom, Resorcinum, Salol, Silicea, Symphytum, Tabacum, Terebinthina, Thyroidinum, Triticum, Zinc Oxyd.

NDC Product Code 64578-0151

NDC CODE: 64578-0151

Proprietary Name: Tox-chord 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: Alfalfa, Alumina, Benzoicum Ac, Carboneum, Cetraria, Folliculinum, Fucus, Fumaricum Ac, Hepar Suis, Kali Carb, Kreosotum, Nat Mur, Paraffinum, Petroleum, Phosphoricum Ac, Phos, Pix Liquida, Plantago, Plumb Met, Pulsatilla, Radium Brom, Resorcinum, Salol, Silicea, Symphytum, Tabacum, Terebinthina, Thyroidinum, Triticum, Zinc Oxyd. 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
  • This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

NDC Code Structure

  • 64578 - Energetix Corporation

NDC 64578-0151-1

Package Description: 59.1 mL in 1 BOTTLE, DROPPER

NDC Product Information

Tox-chord with NDC 64578-0151 is a a human over the counter drug product labeled by Energetix Corporation. The generic name of Tox-chord is alfalfa, alumina, benzoicum ac, carboneum, cetraria, folliculinum, fucus, fumaricum ac, hepar suis, kali carb, kreosotum, nat mur, paraffinum, petroleum, phosphoricum ac, phos, pix liquida, plantago, plumb met, pulsatilla, radium brom, resorcinum, salol, silicea, symphytum, tabacum, terebinthina, thyroidinum, triticum, zinc oxyd.. 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.

Tox-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.

  • ALFALFA 4 [hp_X]/59.1mL
  • ALUMINUM OXIDE 18 [hp_X]/59.1mL
  • BENZOIC ACID 18 [hp_X]/59.1mL
  • D&C BLACK NO. 2 18 [hp_X]/59.1mL
  • CETRARIA ISLANDICA SUBSP. ISLANDICA 9 [hp_C]/59.1mL
  • ESTRONE 18 [hp_X]/59.1mL
  • FUCUS VESICULOSUS 5 [hp_X]/59.1mL
  • FUMARIC ACID 18 [hp_X]/59.1mL
  • PORK LIVER 9 [hp_X]/59.1mL
  • POTASSIUM CARBONATE 12 [hp_X]/59.1mL
  • WOOD CREOSOTE 18 [hp_X]/59.1mL
  • SODIUM CHLORIDE 12 [hp_X]/59.1mL
  • PARAFFIN 18 [hp_X]/59.1mL
  • KEROSENE 18 [hp_X]/59.1mL
  • PHOSPHORIC ACID 12 [hp_X]/59.1mL
  • PHOSPHORUS 12 [hp_X]/59.1mL
  • PINE TAR 18 [hp_X]/59.1mL
  • PLANTAGO MAJOR 4 [hp_X]/59.1mL
  • LEAD 15 [hp_X]/59.1mL
  • PULSATILLA VULGARIS 12 [hp_X]/59.1mL
  • RADIUM BROMIDE 15 [hp_C]/59.1mL
  • RESORCINOL 18 [hp_X]/59.1mL
  • PHENYL SALICYLATE 18 [hp_X]/59.1mL
  • SILICON DIOXIDE 12 [hp_X]/59.1mL
  • COMFREY ROOT 6 [hp_X]/59.1mL
  • TOBACCO LEAF 30 [hp_X]/59.1mL
  • TURPENTINE OIL 18 [hp_X]/59.1mL
  • THYROID, UNSPECIFIED 9 [hp_X]/59.1mL
  • ELYMUS REPENS ROOT 4 [hp_X]/59.1mL
  • ZINC OXIDE 18 [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.

  • ALCOHOL (UNII: 3K9958V90M)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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.
  • 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: 04-01-2017 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.

Tox-chord Product Label Images