64578-0142 NDC - DRAINAGE-TONE (CALCAREA IODATA, CAPSICUM ANNUUM, COENZYME A, ECHINACEA ANGUSTIFOLIA, EQUISETUM ARVENSE, HYDRASTIS CANADENSIS, NADIDUM, NITRICUM ACIDUM, OLEUM MORRHUAE, PETROSELINUM SATIVUM, PHYTOLACCA DECANDRA, SCROPHULARIA NODOSA, SILICEA, SINAPIS ALBA, THUJA OCCIDENTALIS.)

Drug Information

Product NDC: 64578-0142

Proprietary Name: Drainage-Tone

Non Proprietary Name: Calcarea iodata, Capsicum annuum, Coenzyme A, Echinacea angustifolia, Equisetum arvense, Hydrastis canadensis, Nadidum, Nitricum acidum, Oleum morrhuae, Petroselinum sativum, Phytolacca decandra, Scrophularia nodosa, Silicea, Sinapis alba, Thuja occidentalis.

Active Ingredient(s):
  • 12 [hp_X]/59.1mL CALCIUM IODIDE;
  • 6 [hp_X]/59.1mL CAPSICUM;
  • 15 [hp_X]/59.1mL COD LIVER OIL;
  • 8 [hp_X]/59.1mL COENZYME A;
  • 4 [hp_X]/59.1mL ECHINACEA ANGUSTIFOLIA;
  • 6 [hp_X]/59.1mL EQUISETUM ARVENSE TOP;
  • 5 [hp_X]/59.1mL GOLDENSEAL;
  • 8 [hp_X]/59.1mL NADIDE;
  • 12 [hp_X]/59.1mL NITRIC ACID;
  • 4 [hp_X]/59.1mL PETROSELINUM CRISPUM;
  • 4 [hp_X]/59.1mL PHYTOLACCA AMERICANA ROOT;
  • 4 [hp_X]/59.1mL SCROPHULARIA NODOSA;
  • 12 [hp_X]/59.1mL SILICON DIOXIDE;
  • 4 [hp_X]/59.1mL THUJA OCCIDENTALIS LEAFY TWIG;
  • 4 [hp_X]/59.1mL WHITE MUSTARD SEED


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Blood Coagulation Factor [EPC];
  • Calcium [CS];
  • Cations;
  • Divalent [CS];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Coagulation Factor Activity [PE];
  • Increased Histamine Release [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: Energetix Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/31/2017

Package Information

No. Package Code Package Description Billing Unit
164578-0142-159.1 mL in 1 BOTTLE, DROPPER (64578-0142-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0142The 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 NAMEDrainage-ToneThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECalcarea iodata, Capsicum annuum, Coenzyme A, Echinacea angustifolia, Equisetum arvense, Hydrastis canadensis, Nadidum, Nitricum acidum, Oleum morrhuae, Petroselinum sativum, Phytolacca decandra, Scrophularia nodosa, Silicea, Sinapis alba, Thuja occidentalis.The 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 DATE7/31/2017This 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 NAMECALCIUM IODIDE; CAPSICUM; COD LIVER OIL; COENZYME A; ECHINACEA ANGUSTIFOLIA; EQUISETUM ARVENSE TOP; GOLDENSEAL; NADIDE; NITRIC ACID; PETROSELINUM CRISPUM; PHYTOLACCA AMERICANA ROOT; SCROPHULARIA NODOSA; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAFY TWIG; WHITE MUSTARD SEEDAn 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; 6; 15; 8; 4; 6; 5; 8; 12; 4; 4; 4; 12; 4; 4 
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 
PHARM CLASSESAllergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS] 

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