NDC 64578-0153 Lymph-tone Ii

Aesculus Hipp, Azadirachta, Baryta Carb, Berber Vulg, Boldo, Bufo, Calc Carb, Calc Phos, Coenzyme A, Collinsonia, Echinacea, Ferrum Phos, Glandula Suprarenalis Suis, Hypothalamus, Kreosotum, Nadidum, Nat Mur, Phos, Phytolacca, Pinus Syl, Pituitarum Posterium, Pix Liquida, Pulsatilla, Silicea, Stillingia, Thuja Occ.

NDC Product Code 64578-0153

NDC Code: 64578-0153

Proprietary Name: Lymph-tone Ii 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: Aesculus Hipp, Azadirachta, Baryta Carb, Berber Vulg, Boldo, Bufo, Calc Carb, Calc Phos, Coenzyme A, Collinsonia, Echinacea, Ferrum Phos, Glandula Suprarenalis Suis, Hypothalamus, Kreosotum, Nadidum, Nat Mur, Phos, Phytolacca, Pinus Syl, Pituitarum Posterium, Pix Liquida, Pulsatilla, Silicea, Stillingia, Thuja Occ. 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 Corporation

NDC 64578-0153-1

Package Description: 59.1 mL in 1 BOTTLE, DROPPER

NDC Product Information

Lymph-tone Ii with NDC 64578-0153 is a a human over the counter drug product labeled by Energetix Corporation. The generic name of Lymph-tone Ii is aesculus hipp, azadirachta, baryta carb, berber vulg, boldo, bufo, calc carb, calc phos, coenzyme a, collinsonia, echinacea, ferrum phos, glandula suprarenalis suis, hypothalamus, kreosotum, nadidum, nat mur, phos, phytolacca, pinus syl, pituitarum posterium, pix liquida, pulsatilla, silicea, stillingia, thuja occ.. 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.

Lymph-tone Ii 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.

  • HORSE CHESTNUT 12 [hp_X]/59.1mL
  • AZADIRACHTA INDICA BARK 8 [hp_X]/59.1mL
  • BARIUM CARBONATE 12 [hp_X]/59.1mL
  • BERBERIS VULGARIS ROOT BARK 12 [hp_X]/59.1mL
  • PEUMUS BOLDUS LEAF 4 [hp_X]/59.1mL
  • BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/59.1mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/59.1mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/59.1mL
  • COENZYME A 12 [hp_X]/59.1mL
  • COLLINSONIA CANADENSIS ROOT 10 [hp_X]/59.1mL
  • ECHINACEA ANGUSTIFOLIA 6 [hp_X]/59.1mL
  • FERRUM PHOSPHORICUM 12 [hp_X]/59.1mL
  • SUS SCROFA ADRENAL GLAND 9 [hp_X]/59.1mL
  • BOS TAURUS HYPOTHALAMUS 12 [hp_X]/59.1mL
  • WOOD CREOSOTE 15 [hp_X]/59.1mL
  • NADIDE 12 [hp_X]/59.1mL
  • SODIUM CHLORIDE 12 [hp_X]/59.1mL
  • PHOSPHORUS 30 [hp_X]/59.1mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/59.1mL
  • PINUS SYLVESTRIS LEAFY TWIG 9 [hp_X]/59.1mL
  • BOS TAURUS PITUITARY GLAND 12 [hp_X]/59.1mL
  • PINE TAR 6 [hp_X]/59.1mL
  • PULSATILLA VULGARIS 12 [hp_X]/59.1mL
  • SILICON DIOXIDE 12 [hp_X]/59.1mL
  • STILLINGIA SYLVATICA ROOT 4 [hp_X]/59.1mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [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: 11-03-2017 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.

Lymph-tone Ii Product Label Images

Lymph-tone Ii 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.