63479-0407 NDC - D07 (ARANEUS DIADEMATUS, ARISAEMA TRIPHYLLUM ROOT, ASTERIAS RUBENS, BAPTISIA TINCTORIA, BARIUM IODIDE, ECHINACEA ANGUSTIFOLIA, FERROUS IODIDE, GOLDENSEAL, LACHESIS MUTA VENOM, PHYTOLACCA AMERICANA ROOT, PINUS SYLVESTRIS FLOWERING TOP, SCROPHULARIA NODOSA, SPONGIA OFFICINALIS SKELETON, ROASTED, AND TEUCRIUM SCORODONIA FLOWERING TOP)

Drug Information

Product NDC: 63479-0407

Proprietary Name: D07

Non Proprietary Name: araneus diadematus, arisaema triphyllum root, asterias rubens, baptisia tinctoria, barium iodide, echinacea angustifolia, ferrous iodide, goldenseal, lachesis muta venom, phytolacca americana root, pinus sylvestris flowering top, scrophularia nodosa, spongia officinalis skeleton, roasted, and teucrium scorodonia flowering top

Active Ingredient(s):
  • 18 [hp_X]/mL ARANEUS DIADEMATUS;
  • 2 [hp_X]/mL ARISAEMA TRIPHYLLUM ROOT;
  • 6 [hp_X]/mL ASTERIAS RUBENS;
  • 2 [hp_X]/mL BAPTISIA TINCTORIA ROOT;
  • 6 [hp_X]/mL BARIUM IODIDE;
  • 1 [hp_X]/mL ECHINACEA ANGUSTIFOLIA;
  • 12 [hp_X]/mL FERROUS IODIDE;
  • 6 [hp_X]/mL GOLDENSEAL;
  • 30 [hp_X]/mL LACHESIS MUTA VENOM;
  • 30 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 15 [hp_X]/mL PINUS SYLVESTRIS FLOWERING TOP;
  • 2 [hp_X]/mL SCROPHULARIA NODOSA;
  • 30 [hp_X]/mL SPONGIA OFFICINALIS SKELETON, ROASTED;
  • 2 [hp_X]/mL TEUCRIUM SCORODONIA FLOWERING TOP


Administration Route(s): SUBLINGUAL

Dosage Form(s): SOLUTION

Labeler Information

Labeler Name: Apex Energetics Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/1/1988

Package Information

No. Package Code Package Description Billing Unit
163479-0407-130 mL in 1 BOTTLE, GLASS (63479-0407-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63479-0407The 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 NAMED07The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXLMPH-DRNA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMEaraneus diadematus, arisaema triphyllum root, asterias rubens, baptisia tinctoria, barium iodide, echinacea angustifolia, ferrous iodide, goldenseal, lachesis muta venom, phytolacca americana root, pinus sylvestris flowering top, scrophularia nodosa, spongia officinalis skeleton, roasted, and teucrium scorodonia flowering topThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMESUBLINGUALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/1/1988This 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 NAMEApex Energetics Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARANEUS DIADEMATUS; ARISAEMA TRIPHYLLUM ROOT; ASTERIAS RUBENS; BAPTISIA TINCTORIA ROOT; BARIUM IODIDE; ECHINACEA ANGUSTIFOLIA; FERROUS IODIDE; GOLDENSEAL; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS FLOWERING TOP; SCROPHULARIA NODOSA; SPONGIA OFFICINALIS SKELETON, ROASTED; TEUCRIUM SCORODONIA FLOWERING TOPAn 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 STRENGTH18; 2; 6; 2; 6; 1; 12; 6; 30; 30; 15; 2; 30; 2 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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