63479-0104 NDC - A04 (ALLIUM CEPA, ALLIUM SATIVUM, ALOE SOCOTRINA, ARSENICUM IODATUM, ASTERIAS RUBENS, BAPTISIA TINCTORIA, CALCAREA IODATA, CANDIDA ALBICANS, CARBO VEGETABILIS, CHELIDONIUM MAJUS, CINA, CINCHONA OFFICINALIS, COLCHICUM AUTUMNALE, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, INDOLUM, LAC VACCINUM, LACTICUM ACIDUM, MILLEFOLIUM, SACCHARUM OFFICINALE, SARCOLACTICUM ACIDUM, SCROPHULARIA NODOSA, SKATOLUM, SOLIDAGO VIRGAUREA, SULPHUR, URICUM ACIDUM)

Drug Information

  • Product NDC: 63479-0104
  • Proprietary Name: A04
  • Non Proprietary Name: ALLIUM CEPA, ALLIUM SATIVUM, ALOE SOCOTRINA, ARSENICUM IODATUM, ASTERIAS RUBENS, BAPTISIA TINCTORIA, CALCAREA IODATA, CANDIDA ALBICANS, CARBO VEGETABILIS, CHELIDONIUM MAJUS, CINA, CINCHONA OFFICINALIS, COLCHICUM AUTUMNALE, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, INDOLUM, LAC VACCINUM, LACTICUM ACIDUM, MILLEFOLIUM, SACCHARUM OFFICINALE, SARCOLACTICUM ACIDUM, SCROPHULARIA NODOSA, SKATOLUM, SOLIDAGO VIRGAUREA, SULPHUR, URICUM ACIDUM
  • Active Ingredient(s): 1 [hp_X]/mL ACHILLEA MILLEFOLIUM; 12 [hp_X]/mL ACTIVATED CHARCOAL; 15 [hp_X]/mL ALOE; 15 [hp_X]/mL ARSENIC TRIIODIDE; 3 [hp_X]/mL ARTEMISIA CINA PRE-FLOWERING TOP; 8 [hp_X]/mL ASTERIAS RUBENS; 15 [hp_X]/mL BAPTISIA TINCTORIA ROOT; 30 [hp_X]/mL CALCIUM IODIDE; 200 [hp_X]/mL CANDIDA ALBICANS; 30 [hp_X]/mL CHELIDONIUM MAJUS; 3 [hp_X]/mL CINCHONA OFFICINALIS BARK; 30 [hp_X]/mL COLCHICUM AUTUMNALE BULB; 200 [hp_X]/mL COW MILK; 1 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 1 [hp_X]/mL ECHINACEA PURPUREA; 1 [hp_X]/mL GARLIC; 30 [hp_X]/mL INDOLE; 200 [hp_X]/mL LACTIC ACID, DL-; 200 [hp_X]/mL LACTIC ACID, L-; 1 [hp_X]/mL ONION; 30 [hp_X]/mL SCROPHULARIA NODOSA; 30 [hp_X]/mL SKATOLE; 1 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP; 200 [hp_X]/mL SUCROSE; 12 [hp_X]/mL SULFUR; 15 [hp_X]/mL URIC ACID
  • Administration Route(s): SUBLINGUAL
  • Dosage Form(s): SOLUTION/ DROPS
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Blood Coagulation Factor [EPC]; Calcium [CS]; Cations; Divalent [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Dietary Proteins [CS]; Fungal Proteins [CS]; Increased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Milk Proteins [CS]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Plant Proteins [CS]; Vegetable Proteins [CS]

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:12/15/1994

Package Information

No. Package Code Package Description Billing Unit
163479-0104-130 mL in 1 BOTTLE, GLASS (63479-0104-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63479-0104The 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 NAMEA04The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXDEEP ANTITOXA 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 NAMEALLIUM CEPA, ALLIUM SATIVUM, ALOE SOCOTRINA, ARSENICUM IODATUM, ASTERIAS RUBENS, BAPTISIA TINCTORIA, CALCAREA IODATA, CANDIDA ALBICANS, CARBO VEGETABILIS, CHELIDONIUM MAJUS, CINA, CINCHONA OFFICINALIS, COLCHICUM AUTUMNALE, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, INDOLUM, LAC VACCINUM, LACTICUM ACIDUM, MILLEFOLIUM, SACCHARUM OFFICINALE, SARCOLACTICUM ACIDUM, SCROPHULARIA NODOSA, SKATOLUM, SOLIDAGO VIRGAUREA, SULPHUR, URICUM ACIDUMThe 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 DATE12/15/1994This 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 NAMEACHILLEA MILLEFOLIUM; ACTIVATED CHARCOAL; ALOE; ARSENIC TRIIODIDE; ARTEMISIA CINA PRE-FLOWERING TOP; ASTERIAS RUBENS; BAPTISIA TINCTORIA ROOT; CALCIUM IODIDE; CANDIDA ALBICANS; CHELIDONIUM MAJUS; CINCHONA OFFICINALIS BARK; COLCHICUM AUTUMNALE BULB; COW MILK; ECHINACEA ANGUSTIFOLIA WHOLE; ECHINACEA PURPUREA; GARLIC; INDOLE; LACTIC ACID, DL-; LACTIC ACID, L-; ONION; SCROPHULARIA NODOSA; SKATOLE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUCROSE; SULFUR; URIC ACIDAn 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 STRENGTH1; 12; 15; 15; 3; 8; 15; 30; 200; 30; 3; 30; 200; 1; 1; 1; 30; 200; 200; 1; 30; 30; 1; 200; 12; 15 
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; [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], Allergens [CS], Allergens [CS], Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Dietary Proteins [CS], Fungal Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Milk Proteins [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Plant Proteins [CS], Vegetable Proteins [CS] 

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

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