63479-0409 NDC - D09 (AMBROSIA ARTEMISIAEFOLIA, ARALIA RACEMOSA, ARNICA MONTANA, CALENDULA OFFICINALIS, CHROMICUM ACIDUM, ECHINACEA PURPUREA, EUCALYPTOL, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC VACCINUM, MERCURIUS IODATUS FLAVUS, MERCURIUS SULPHURATUS RUBER, NATRUM ARSENICICUM, ROSA DAMASCENA, SABADILLA, SANGUINARINUM NITRICUM, SYMPHYTUM OFFICINALE)

Drug Information

  • Product NDC: 63479-0409
  • Proprietary Name: D09
  • Non Proprietary Name: AMBROSIA ARTEMISIAEFOLIA, ARALIA RACEMOSA, ARNICA MONTANA, CALENDULA OFFICINALIS, CHROMICUM ACIDUM, ECHINACEA PURPUREA, EUCALYPTOL, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC VACCINUM, MERCURIUS IODATUS FLAVUS, MERCURIUS SULPHURATUS RUBER, NATRUM ARSENICICUM, ROSA DAMASCENA, SABADILLA, SANGUINARINUM NITRICUM, SYMPHYTUM OFFICINALE
  • Active Ingredient(s): 3 [hp_X]/mL AMBROSIA ARTEMISIIFOLIA; 3 [hp_X]/mL ARALIA RACEMOSA ROOT; 9 [hp_X]/mL ARNICA MONTANA; 2 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP; 8 [hp_X]/mL CHROMIUM TRIOXIDE; 8 [hp_X]/mL COMFREY ROOT; 15 [hp_X]/mL COW MILK; 1 [hp_X]/mL ECHINACEA PURPUREA; 4 [hp_X]/mL EUCALYPTOL; 8 [hp_X]/mL MERCURIC SULFIDE; 8 [hp_X]/mL MERCUROUS IODIDE; 8 [hp_X]/mL POTASSIUM CHLORIDE; 8 [hp_X]/mL POTASSIUM DICHROMATE; 8 [hp_X]/mL POTASSIUM SULFATE; 3 [hp_X]/mL ROSA DAMASCENA FLOWERING TOP; 8 [hp_X]/mL SANGUINARINE NITRATE; 6 [hp_X]/mL SCHOENOCAULON OFFICINALE SEED; 8 [hp_X]/mL SODIUM ARSENATE, DIBASIC, HEPTAHYDRATE
  • Administration Route(s): SUBLINGUAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Large Intestinal Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Milk Proteins [CS]; Non-Standardized Food Allergenic Extract [EPC]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Compounds [CS]; Potassium Salt [EPC]; Potassium Salt [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Apex Energetics Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/15/1993

Package Information

No. Package Code Package Description Billing Unit
163479-0409-130 mL in 1 BOTTLE, GLASS (63479-0409-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63479-0409The 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 NAMED09The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXSNS-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 NAMEAMBROSIA ARTEMISIAEFOLIA, ARALIA RACEMOSA, ARNICA MONTANA, CALENDULA OFFICINALIS, CHROMICUM ACIDUM, ECHINACEA PURPUREA, EUCALYPTOL, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC VACCINUM, MERCURIUS IODATUS FLAVUS, MERCURIUS SULPHURATUS RUBER, NATRUM ARSENICICUM, ROSA DAMASCENA, SABADILLA, SANGUINARINUM NITRICUM, SYMPHYTUM OFFICINALEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe 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 DATE3/15/1993This 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 NAMEAMBROSIA ARTEMISIIFOLIA; ARALIA RACEMOSA ROOT; ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; CHROMIUM TRIOXIDE; COMFREY ROOT; COW MILK; ECHINACEA PURPUREA; EUCALYPTOL; MERCURIC SULFIDE; MERCUROUS IODIDE; POTASSIUM CHLORIDE; POTASSIUM DICHROMATE; POTASSIUM SULFATE; ROSA DAMASCENA FLOWERING TOP; SANGUINARINE NITRATE; SCHOENOCAULON OFFICINALE SEED; SODIUM ARSENATE, DIBASIC, HEPTAHYDRATEAn 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 STRENGTH3; 3; 9; 2; 8; 8; 15; 1; 4; 8; 8; 8; 8; 8; 3; 8; 6; 8 
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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Milk Proteins [CS], Non-Standardized Food Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC] 

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This page was last updated on: 12/6/2025

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