63479-0308 NDC - C08 (ABIES ALBA LEAFY TWIG, CALCAREA ACETICA, CALCAREA ARSENICICA, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA HYPOPHOSPHOROSA, CALCAREA IODATA, CALCAREA MURIATICA, CALCAREA OXALICA, CALCAREA PHOSPHORICA, CALCAREA PICRATA, CALCAREA SULPHURICA, CALCULUS BOVIS, CALENDULA OFFICINALIS, CHOLESTERINUM, HAMAMELIS VIRGINIANA, HEPAR SULPHURIS CALCAREUM, LAPIS ALBUS, SILICEA, SULPHUR IODATUM, SUS SCROFA PARATHYROID GLAND, SYMPHYTUM OFFICINALE, URTICA URENS, VITAMIN D)

Drug Information

Product NDC: 63479-0308

Proprietary Name: C08

Non Proprietary Name: ABIES ALBA LEAFY TWIG, CALCAREA ACETICA, CALCAREA ARSENICICA, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA HYPOPHOSPHOROSA, CALCAREA IODATA, CALCAREA MURIATICA, CALCAREA OXALICA, CALCAREA PHOSPHORICA, CALCAREA PICRATA, CALCAREA SULPHURICA, CALCULUS BOVIS, CALENDULA OFFICINALIS, CHOLESTERINUM, HAMAMELIS VIRGINIANA, HEPAR SULPHURIS CALCAREUM, LAPIS ALBUS, SILICEA, SULPHUR IODATUM, SUS SCROFA PARATHYROID GLAND, SYMPHYTUM OFFICINALE, URTICA URENS, VITAMIN D

Active Ingredient(s):
  • 8 [hp_X]/mL ABIES ALBA LEAFY TWIG;
  • 15 [hp_X]/mL BOS TAURUS GALLSTONE;
  • 12 [hp_X]/mL CALCIUM ACETATE;
  • 8 [hp_X]/mL CALCIUM ARSENATE;
  • 12 [hp_X]/mL CALCIUM CHLORIDE;
  • 15 [hp_X]/mL CALCIUM FLUORIDE;
  • 12 [hp_X]/mL CALCIUM HEXAFLUOROSILICATE;
  • 12 [hp_X]/mL CALCIUM HYPOPHOSPHITE;
  • 12 [hp_X]/mL CALCIUM IODIDE;
  • 12 [hp_X]/mL CALCIUM OXALATE MONOHYDRATE;
  • 12 [hp_X]/mL CALCIUM PICRATE;
  • 12 [hp_X]/mL CALCIUM SULFATE ANHYDROUS;
  • 15 [hp_X]/mL CALCIUM SULFIDE;
  • 6 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP;
  • 15 [hp_X]/mL CHOLESTEROL;
  • 6 [hp_X]/mL COMFREY ROOT;
  • 6 [hp_X]/mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK;
  • 15 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 12 [hp_X]/mL SILICON DIOXIDE;
  • 12 [hp_X]/mL SULFUR IODIDE;
  • 9 [hp_C]/mL SUS SCROFA PARATHYROID GLAND;
  • 15 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE;
  • 12 [hp_X]/mL URTICA URENS;
  • 12 [hp_X]/mL VITAMIN D


Administration Route(s): SUBLINGUAL

Dosage Form(s): SOLUTION/ DROPS

Pharmacy Class(es):
  • Blood Coagulation Factor [EPC];
  • Blood Coagulation Factor [EPC];
  • Blood Coagulation Factor [EPC];
  • Blood Coagulation Factor [EPC];
  • Blood Coagulation Factor [EPC];
  • Blood Coagulation Factor [EPC];
  • Calcium [CS];
  • Calcium [CS];
  • Calcium [CS];
  • Calcium [CS];
  • Calcium [CS];
  • Calcium [CS];
  • Cations;
  • Divalent [CS];
  • Cations;
  • Divalent [CS];
  • Cations;
  • Divalent [CS];
  • Cations;
  • Divalent [CS];
  • Cations;
  • Divalent [CS];
  • Cations;
  • Divalent [CS];
  • Increased Coagulation Factor Activity [PE];
  • Increased Coagulation Factor Activity [PE];
  • Increased Coagulation Factor Activity [PE];
  • Increased Coagulation Factor Activity [PE];
  • Increased Coagulation Factor Activity [PE];
  • Increased Coagulation Factor Activity [PE]

Labeler Information

Labeler Name: Apex Energetics Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/15/1988

Package Information

No. Package Code Package Description Billing Unit
163479-0308-130 mL in 1 BOTTLE, GLASS (63479-0308-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63479-0308The 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 NAMEC08The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXCALCIUM METABOLISMA 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 NAMEABIES ALBA LEAFY TWIG, CALCAREA ACETICA, CALCAREA ARSENICICA, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA HYPOPHOSPHOROSA, CALCAREA IODATA, CALCAREA MURIATICA, CALCAREA OXALICA, CALCAREA PHOSPHORICA, CALCAREA PICRATA, CALCAREA SULPHURICA, CALCULUS BOVIS, CALENDULA OFFICINALIS, CHOLESTERINUM, HAMAMELIS VIRGINIANA, HEPAR SULPHURIS CALCAREUM, LAPIS ALBUS, SILICEA, SULPHUR IODATUM, SUS SCROFA PARATHYROID GLAND, SYMPHYTUM OFFICINALE, URTICA URENS, VITAMIN DThe 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 DATE8/15/1988This 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 NAMEABIES ALBA LEAFY TWIG; BOS TAURUS GALLSTONE; CALCIUM ACETATE; CALCIUM ARSENATE; CALCIUM CHLORIDE; CALCIUM FLUORIDE; CALCIUM HEXAFLUOROSILICATE; CALCIUM HYPOPHOSPHITE; CALCIUM IODIDE; CALCIUM OXALATE MONOHYDRATE; CALCIUM PICRATE; CALCIUM SULFATE ANHYDROUS; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; CHOLESTEROL; COMFREY ROOT; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SILICON DIOXIDE; SULFUR IODIDE; SUS SCROFA PARATHYROID GLAND; TRIBASIC CALCIUM PHOSPHATE; URTICA URENS; VITAMIN DAn 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 STRENGTH8; 15; 12; 8; 12; 15; 12; 12; 12; 12; 12; 12; 15; 6; 15; 6; 6; 15; 12; 12; 9; 15; 12; 12 
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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESBlood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Calcium [CS], Calcium [CS], Calcium [CS], Calcium [CS], Cations, Divalent [CS], Cations, Divalent [CS], Cations, Divalent [CS], Cations, Divalent [CS], Cations, Divalent [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE] 

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