43857-0168 NDC - FOOD ADDITIVES (BERBERIS VULGARIS, CHELIDONIUM MAJUS, TRIFOLIUM PRATENSE, GLYCYRRHIZA GLABRA, LAPPA MAJOR, PHYTOLACCA DECANDRA, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, XANTHOXYLUM FRAXINEUM, ARSENICUM ALBUM, BELLADONNA, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM)

Drug Information

  • Product NDC: 43857-0168
  • Proprietary Name: Food Additives
  • Non Proprietary Name: Berberis Vulgaris, Chelidonium Majus, Trifolium Pratense, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Stillingia Sylvatica, Xanthoxylum Fraxineum, Arsenicum Album, Belladonna, Lycopodium Clavatum, Natrum Sulphuricum, Phosphoricum Acidum
  • Active Ingredient(s): 4 [hp_X]/mL ARCTIUM LAPPA ROOT; 12 [hp_X]/mL ARSENIC TRIOXIDE; 12 [hp_X]/mL ATROPA BELLADONNA WHOLE; 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK; 3 [hp_X]/mL CHELIDONIUM MAJUS; 4 [hp_X]/mL FRANGULA ALNUS BARK; 4 [hp_X]/mL FRANGULA PURSHIANA BARK; 4 [hp_X]/mL GLYCYRRHIZA GLABRA; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 12 [hp_X]/mL PHOSPHORIC ACID; 4 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 12 [hp_X]/mL SODIUM SULFATE; 4 [hp_X]/mL STILLINGIA SYLVATICA ROOT; 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER; 4 [hp_X]/mL ZANTHOXYLUM AMERICANUM BARK
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]

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:5/16/2013

Package Information

No. Package Code Package Description Billing Unit
143857-0168-130 mL in 1 BOTTLE, DROPPER (43857-0168-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0168The 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 NAMEFood AdditivesThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBerberis Vulgaris, Chelidonium Majus, Trifolium Pratense, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Stillingia Sylvatica, Xanthoxylum Fraxineum, Arsenicum Album, Belladonna, Lycopodium Clavatum, Natrum Sulphuricum, Phosphoricum AcidumThe 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 DATE5/16/2013This 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 NAMEBioActive Nutritional, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARCTIUM LAPPA ROOT; ARSENIC TRIOXIDE; ATROPA BELLADONNA WHOLE; BERBERIS VULGARIS ROOT BARK; CHELIDONIUM MAJUS; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; GLYCYRRHIZA GLABRA; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; SODIUM SULFATE; STILLINGIA SYLVATICA ROOT; TRIFOLIUM PRATENSE FLOWER; ZANTHOXYLUM AMERICANUM BARKAn 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 STRENGTH4; 12; 12; 3; 3; 4; 4; 4; 12; 12; 4; 12; 4; 3; 4 
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 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 7/4/2025

Previous Code
Next Code