43857-0285 NDC - HA HP (BELLADONNA, BRYONIA (ALBA), GELSEMIUM SEMPERVIRENS, GLONOINUM, MELILOTUS OFFICINALIS, NUX VOMICA, SILICEA, SPIGELIA ANTHELMIA)

Drug Information

  • Product NDC: 43857-0285
  • Proprietary Name: HA HP
  • Non Proprietary Name: Belladonna, Bryonia (Alba), Gelsemium Sempervirens, Glonoinum, Melilotus Officinalis, Nux Vomica, Silicea, Spigelia Anthelmia
  • Active Ingredient(s): 30 [hp_X]/mL ATROPA BELLADONNA; 30 [hp_X]/mL BRYONIA ALBA ROOT; 30 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT; 30 [hp_X]/mL MELILOTUS OFFICINALIS TOP; 30 [hp_X]/mL NITROGLYCERIN; 30 [hp_X]/mL SILICON DIOXIDE; 30 [hp_X]/mL SODIUM CHLORIDE; 30 [hp_X]/mL SPIGELIA ANTHELMIA; 30 [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]; Nitrate Vasodilator [EPC]; Nitrates [CS]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Vasodilation [PE]

Labeler Information

Field Name Field Value
Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/22/2014

Package Information

No. Package Code Package Description Billing Unit
143857-0285-130 mL in 1 BOTTLE, DROPPER (43857-0285-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0285The 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 NAMEHA HPThe 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.
NON PROPRIETARY NAMEBelladonna, Bryonia (Alba), Gelsemium Sempervirens, Glonoinum, Melilotus Officinalis, Nux Vomica, Silicea, Spigelia AnthelmiaThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThis is the date that the labeler indicates was the start of its marketing of the drug product.
ROUTE NAMEORALThis 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.
START MARKETING DATE8/22/2014Product 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.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICName of Company corresponding to the labeler code segment of the Product NDC.
LABELER NAMEBioActive Nutritional, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEATROPA BELLADONNA; BRYONIA ALBA ROOT; GELSEMIUM SEMPERVIRENS ROOT; MELILOTUS OFFICINALIS TOP; NITROGLYCERIN; SILICON DIOXIDE; SODIUM CHLORIDE; SPIGELIA ANTHELMIA; 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 STRENGTH30; 30; 30; 30; 30; 30; 30; 30; 30 
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 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vasodilation [PE] 

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

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