45341-0002 NDC - ARTALGIA (CARDUUS MARIANUS, ARNICA MONTANA, AGARICUS MUSCARIUS, BARYTA CARBONICA, BELLIS PERENNIS, GLONOINUM, HAMAMELIS VIRGINIANA, MERCURIUS SOLUBILIS, PLUMBUM METALLICUM, SECALE CORNUTUM, VANADIUM METALLICUM, CARBO VEGETABILIS, HYPERICUM PERFORATUM, PHOSPHORUS PULSATILLA (PRATENSIS), RHUS TOX)

Drug Information

  • Product NDC: 45341-0002
  • Proprietary Name: Artalgia
  • Non Proprietary Name: Carduus Marianus, Arnica Montana, Agaricus Muscarius, Baryta Carbonica, Bellis Perennis, Glonoinum, Hamamelis Virginiana, Mercurius Solubilis, Plumbum Metallicum, Secale Cornutum, Vanadium Metallicum, Carbo Vegetabilis, Hypericum Perforatum, Phosphorus Pulsatilla (Pratensis), Rhus Tox
  • Active Ingredient(s): 30 [hp_X]/mL ACTIVATED CHARCOAL; 12 [hp_X]/mL AMANITA MUSCARIA FRUITING BODY; 3 [hp_X]/mL ARNICA MONTANA WHOLE; 12 [hp_X]/mL BARIUM CARBONATE; 12 [hp_X]/mL BELLIS PERENNIS WHOLE; 12 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM; 12 [hp_X]/mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; 30 [hp_X]/mL HYPERICUM PERFORATUM WHOLE; 12 [hp_X]/mL LEAD; 12 [hp_X]/mL MERCURIUS SOLUBILIS; 3 [hp_X]/mL MILK THISTLE; 12 [hp_X]/mL NITROGLYCERIN; 30 [hp_X]/mL PHOSPHORUS; 30 [hp_X]/mL PULSATILLA PRATENSIS WHOLE; 30 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF; 12 [hp_X]/mL VANADIUM
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Nitrate Vasodilator [EPC]; Nitrates [CS]; Vasodilation [PE]

Labeler Information

Field Name Field Value
Labeler Name: Todd Horton DPM
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/15/2020

Package Information

No. Package Code Package Description Billing Unit
145341-0002-130 mL in 1 BOTTLE, DROPPER (45341-0002-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC45341-0002The 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 NAMEArtalgiaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECarduus Marianus, Arnica Montana, Agaricus Muscarius, Baryta Carbonica, Bellis Perennis, Glonoinum, Hamamelis Virginiana, Mercurius Solubilis, Plumbum Metallicum, Secale Cornutum, Vanadium Metallicum, Carbo Vegetabilis, Hypericum Perforatum, Phosphorus Pulsatilla (Pratensis), Rhus ToxThe 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 DATE7/15/2020This 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 NAMETodd Horton DPMName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACTIVATED CHARCOAL; AMANITA MUSCARIA FRUITING BODY; ARNICA MONTANA WHOLE; BARIUM CARBONATE; BELLIS PERENNIS WHOLE; CLAVICEPS PURPUREA SCLEROTIUM; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM WHOLE; LEAD; MERCURIUS SOLUBILIS; MILK THISTLE; NITROGLYCERIN; PHOSPHORUS; PULSATILLA PRATENSIS WHOLE; TOXICODENDRON PUBESCENS LEAF; VANADIUMAn 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 STRENGTH30; 12; 3; 12; 12; 12; 12; 30; 12; 12; 3; 12; 30; 30; 30; 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 
PHARM CLASSESNitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE] 

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This page was last updated on: 1/16/2026

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