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NDC 70321-0003 Energize

Colchicum Autumnale,Conium Maculatum,Hydrastis Canadensis,Vaccinium Myrtillus,Podophyllum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70321-0003?
  4. Energize Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
70321-0003
Proprietary Name:
Energize
Non-Proprietary Name: [1]
Colchicum Autumnale, Conium Maculatum, Hydrastis Canadensis, Vaccinium Myrtillus, Podophyllum Peltatum, Ascorbic Acid, Galium Aparine, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Norepinephrine, Alpha-lipoicum Acidum, Natrum Oxalaceticum, Sulphur, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthrachinonum, Histaminum Hydrochloricum, Magnesium Gluconicum Dihydricum, Nadidum, Naphthochinonum, Pantothenic Acid
Substance Name: [2]
1,4-naphthoquinone; Adenosine Triphosphate Disodium; Ascorbic Acid; Aspirin; Bacillus Anthracis Immunoserum Rabbit; Bilberry; Colchicum Autumnale Bulb; Conium Maculatum Flowering Top; Galium Aparine; Goldenseal; Histamine Dihydrochloride; Hydroquinine; Lactic Acid, L-; Magnesium Gluconate; Manganese Phosphate, Dibasic; Nadide; Niacinamide; Norepinephrine; Pantothenic Acid; Podophyllum; Pyridoxine Hydrochloride; Riboflavin; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Sodium Diethyl Oxalacetate; Sulfur; Thiamine Hydrochloride; Thioctic Acid; Ubidecarenone
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Parasitology Center Inc.
    Labeler Code:
    70321
    Product Label ID:
    1228bfab-6e51-4295-8194-5f2b395d62d2
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    04-27-2016
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 70321-0003-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 70321-0003?

    The NDC code 70321-0003 is assigned by the FDA to the product Energize which is a human over the counter drug product labeled by Parasitology Center Inc.. The generic name of Energize is colchicum autumnale, conium maculatum, hydrastis canadensis, vaccinium myrtillus, podophyllum peltatum, ascorbic acid, galium aparine, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, sarcolacticum acidum, thiaminum hydrochloricum, norepinephrine, alpha-lipoicum acidum, natrum oxalaceticum, sulphur, acetylsalicylicum acidum, adenosinum triphosphoricum dinatrum, anthrachinonum, histaminum hydrochloricum, magnesium gluconicum dihydricum, nadidum, naphthochinonum, pantothenic acid. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 70321-0003-1 30 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 and RxNorm crosswalk.

    What are the uses for Energize?

    For temporary relief of exhaustion, fatigue, and feelings of low energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of exhaustion, fatigue, and feelings of low energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Energize Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • 1,4-NAPHTHOQUINONE 10 [hp_X]/mL
    • ADENOSINE TRIPHOSPHATE DISODIUM 10 [hp_X]/mL
    • ASCORBIC ACID 6 [hp_X]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
    • ASPIRIN 10 [hp_X]/mL - The prototypical analgesic used in the treatment of mild to moderate pain. It has anti-inflammatory and antipyretic properties and acts as an inhibitor of cyclooxygenase which results in the inhibition of the biosynthesis of prostaglandins. Aspirin also inhibits platelet aggregation and is used in the prevention of arterial and venous thrombosis. (From Martindale, The Extra Pharmacopoeia, 30th ed, p5)
    • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 10 [hp_X]/mL
    • BILBERRY 4 [hp_X]/mL
    • COLCHICUM AUTUMNALE BULB 4 [hp_X]/mL
    • CONIUM MACULATUM FLOWERING TOP 4 [hp_X]/mL
    • GALIUM APARINE 6 [hp_X]/mL - A genus of herbaceous annual and perennial plants in the family RUBIACEAE.
    • GOLDENSEAL 4 [hp_X]/mL
    • HISTAMINE DIHYDROCHLORIDE 10 [hp_X]/mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
    • HYDROQUININE 3 [hp_C]/mL
    • LACTIC ACID, L- 6 [hp_X]/mL
    • MAGNESIUM GLUCONATE 10 [hp_X]/mL
    • MANGANESE PHOSPHATE, DIBASIC 15 [hp_X]/mL
    • NADIDE 10 [hp_X]/mL
    • NIACINAMIDE 6 [hp_X]/mL - An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
    • NOREPINEPHRINE 6 [hp_X]/mL - Precursor of epinephrine that is secreted by the ADRENAL MEDULLA and is a widespread central and autonomic neurotransmitter. Norepinephrine is the principal transmitter of most postganglionic sympathetic fibers, and of the diffuse projection system in the brain that arises from the LOCUS CERULEUS. It is also found in plants and is used pharmacologically as a sympathomimetic.
    • PANTOTHENIC ACID 10 [hp_X]/mL - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.
    • PODOPHYLLUM 5 [hp_X]/mL - A genus of poisonous American herbs, family BERBERIDACEAE. The roots yield PODOPHYLLOTOXIN and other pharmacologically important agents. The plant was formerly used as a cholagogue and cathartic. It is different from the European mandrake, MANDRAGORA.
    • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
    • RIBOFLAVIN 6 [hp_X]/mL - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.
    • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
    • SODIUM DIETHYL OXALACETATE 8 [hp_X]/mL
    • SULFUR 8 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
    • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL
    • THIOCTIC ACID 8 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
    • UBIDECARENONE 10 [hp_X]/mL

    Which are Energize UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Energize 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. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Energize?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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] 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".