44911-0508 NDC - VASCULAR (AESCULUS HIPPOCASTANUM, COLLINSONIA CANADENSIS, ECHINACEA (ANGUSTIFOLIA), HAMAMELIS VIRGINIANA, PULSATILLA (PRATENSIS), ARNICA MONTANA, CARBO VEGETABILIS, GRAPHITES, HYDROFLUORICUM ACIDUM, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PAEONIA OFFICINALIS, SEPIA)

Drug Information

  • Product NDC: 44911-0508
  • Proprietary Name: Vascular
  • Non Proprietary Name: Aesculus Hippocastanum, Collinsonia Canadensis, Echinacea (Angustifolia), Hamamelis Virginiana, Pulsatilla (Pratensis), Arnica Montana, Carbo Vegetabilis, Graphites, Hydrofluoricum Acidum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Paeonia Officinalis, Sepia
  • Active Ingredient(s): 12 [hp_X]/mL ACTIVATED CHARCOAL; 12 [hp_X]/mL ARNICA MONTANA WHOLE; 3 [hp_X]/mL COLLINSONIA CANADENSIS ROOT; 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 12 [hp_X]/mL GRAPHITE; 3 [hp_X]/mL HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; 3 [hp_X]/mL HORSE CHESTNUT; 12 [hp_X]/mL HYDROFLUORIC ACID; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 12 [hp_X]/mL NITRIC ACID; 12 [hp_X]/mL PAEONIA OFFICINALIS ROOT; 4 [hp_X]/mL PULSATILLA PRATENSIS WHOLE; 12 [hp_X]/mL SEPIA OFFICINALIS JUICE; 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Energique, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/6/2019
End Marketing Date:7/26/2028

Package Information

No. Package Code Package Description Billing Unit
144911-0508-130 mL in 1 BOTTLE, DROPPER (44911-0508-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0508The 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 NAMEVascularThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXHPA 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 NAMEAesculus Hippocastanum, Collinsonia Canadensis, Echinacea (Angustifolia), Hamamelis Virginiana, Pulsatilla (Pratensis), Arnica Montana, Carbo Vegetabilis, Graphites, Hydrofluoricum Acidum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Paeonia Officinalis, SepiaThe 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 DATE8/6/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE7/26/2028This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
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 NAMEEnergique, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACTIVATED CHARCOAL; ARNICA MONTANA WHOLE; COLLINSONIA CANADENSIS ROOT; ECHINACEA ANGUSTIFOLIA WHOLE; GRAPHITE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HORSE CHESTNUT; HYDROFLUORIC ACID; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; PAEONIA OFFICINALIS ROOT; PULSATILLA PRATENSIS WHOLE; SEPIA OFFICINALIS JUICE; STRYCHNOS NUX-VOMICA SEEDAn 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 STRENGTH12; 12; 3; 3; 12; 3; 3; 12; 12; 12; 12; 4; 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 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS] 

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This page was last updated on: 11/21/2025

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