64578-0109 NDC - ISOPATHIC PHENOLIC RINGS (HOMEOPATHIC LIQUID)

Drug Information

Product NDC: 64578-0109

Proprietary Name: Isopathic Phenolic Rings

Non Proprietary Name: Homeopathic Liquid

Active Ingredient(s):
  • 12 [hp_X]/59.1mL ACETALDEHYDE;
  • 12 [hp_X]/59.1mL ANHYDROUS CITRIC ACID;
  • 12 [hp_X]/59.1mL ARABICA COFFEE BEAN;
  • 12 [hp_X]/59.1mL BENZENE;
  • 12 [hp_X]/59.1mL BOS TAURUS HYPOTHALAMUS;
  • 12 [hp_X]/59.1mL BOS TAURUS TESTICLE;
  • 12 [hp_X]/59.1mL CAFFEINE;
  • 12 [hp_X]/59.1mL CANDIDA ALBICANS;
  • 12 [hp_X]/59.1mL CHOLINE;
  • 12 [hp_X]/59.1mL CINNAMON;
  • 12 [hp_X]/59.1mL COCOA;
  • 12 [hp_X]/59.1mL COUMARIN;
  • 12 [hp_X]/59.1mL ESTRONE;
  • 12 [hp_X]/59.1mL GALLIC ACID;
  • 12 [hp_X]/59.1mL GREEN PEPPERCORN;
  • 12 [hp_X]/59.1mL HISTAMINE;
  • 12 [hp_X]/59.1mL INDOLE;
  • 12 [hp_X]/59.1mL KEROSENE;
  • 12 [hp_X]/59.1mL ONION;
  • 12 [hp_X]/59.1mL PETROSELINUM CRISPUM;
  • 12 [hp_X]/59.1mL PHENOL;
  • 12 [hp_X]/59.1mL PHLORIZIN;
  • 12 [hp_X]/59.1mL PHOSPHORUS;
  • 12 [hp_X]/59.1mL SUCROSE;
  • 9 [hp_X]/59.1mL SUS SCROFA ADRENAL GLAND;
  • 12 [hp_X]/59.1mL TURPENTINE OIL;
  • 12 [hp_X]/59.1mL VALERIAN


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Acidifying Activity [MoA];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Anti-coagulant [EPC];
  • Calcium Chelating Activity [MoA];
  • Calculi Dissolution Agent [EPC];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Central Nervous System Stimulant [EPC];
  • Central Nervous System Stimulation [PE];
  • Decreased Coagulation Factor Activity [PE];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Food Additives [CS];
  • Fungal Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Methylxanthine [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Fungal Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS];
  • Vegetable Proteins [CS];
  • Xanthines [CS]

Labeler Information

Labeler Name: Energetix Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/3/2017

Package Information

No. Package Code Package Description Billing Unit
164578-0109-159.1 mL in 1 BOTTLE, DROPPER (64578-0109-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0109The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEIsopathic Phenolic RingsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEHomeopathic LiquidThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/3/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEEnergetix CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACETALDEHYDE; ANHYDROUS CITRIC ACID; ARABICA COFFEE BEAN; BENZENE; BOS TAURUS HYPOTHALAMUS; BOS TAURUS TESTICLE; CAFFEINE; CANDIDA ALBICANS; CHOLINE; CINNAMON; COCOA; COUMARIN; ESTRONE; GALLIC ACID; GREEN PEPPERCORN; HISTAMINE; INDOLE; KEROSENE; ONION; PETROSELINUM CRISPUM; PHENOL; PHLORIZIN; PHOSPHORUS; SUCROSE; SUS SCROFA ADRENAL GLAND; TURPENTINE OIL; VALERIANAn 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.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 9; 12; 12 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL 
PHARM CLASSESAcidifying Activity [MoA], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Decreased Coagulation Factor Activity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Methylxanthine [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS], Xanthines [CS] 

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This page was last updated on: 2/1/2023