43857-0576 NDC - B FORCE (ECHINACEA ANGUSTIFOLIA, LOMATIUM DISSECTUM, MYRRHA, NASTURTIUM AQUATICUM, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, PROPOLIS, GLANDULA SUPRARENALIS SUIS, LYMPH NODE (SUIS), SPLEEN (SUIS), THYMUS (SUIS), THYROIDINUM (SUIS), ARSENICUM ALBUM, BELLADONNA, HYPERICUM PERFORATUM, PHOSPHORUS, BOTULINUM, COLIBACILLINUM CUM NATRUM MURIATICUM, PROTEUS (VULGARIS), PSEUDOMONAS AERUGINOSA, PROTEUS (MORGANI), SALMONELLA TYPHI NOSODE, CLOSTRIDIUM PERFRINGENS)

Drug Information

Product NDC: 43857-0576

Proprietary Name: B Force

Non Proprietary Name: Echinacea Angustifolia, Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Tabebuia Impetiginosa, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Lymph Node (Suis), Spleen (Suis), Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Belladonna, Hypericum Perforatum, Phosphorus, Botulinum, Colibacillinum Cum Natrum Muriaticum, Proteus (Vulgaris), Pseudomonas Aeruginosa, Proteus (Morgani), Salmonella Typhi Nosode, Clostridium Perfringens

Active Ingredient(s):
  • 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE;
  • 3 [hp_X]/mL LOMATIUM DISSECTUM ROOT;
  • 3 [hp_X]/mL MYRRH;
  • 3 [hp_X]/mL NASTURTIUM OFFICINALE;
  • 3 [hp_X]/mL HANDROANTHUS IMPETIGINOSUS BARK;
  • 5 [hp_X]/mL GOLDENSEAL;
  • 6 [hp_X]/mL PROPOLIS WAX;
  • 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND;
  • 8 [hp_X]/mL SUS SCROFA LYMPH;
  • 8 [hp_X]/mL SUS SCROFA SPLEEN;
  • 8 [hp_X]/mL SUS SCROFA THYMUS;
  • 8 [hp_X]/mL SUS SCROFA THYROID;
  • 12 [hp_X]/mL ARSENIC TRIOXIDE;
  • 12 [hp_X]/mL ATROPA BELLADONNA;
  • 12 [hp_X]/mL HYPERICUM PERFORATUM WHOLE;
  • 12 [hp_X]/mL PHOSPHORUS;
  • 30 [hp_X]/mL BOTULINUM TOXIN TYPE A;
  • 30 [hp_X]/mL ESCHERICHIA COLI;
  • 30 [hp_X]/mL PROTEUS VULGARIS;
  • 30 [hp_X]/mL PSEUDOMONAS AERUGINOSA;
  • 30 [hp_X]/mL PROTEUS MORGANII;
  • 33 [hp_X]/mL SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI;
  • 15 [hp_C]/mL CLOSTRIDIUM PERFRINGENS


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/4/2021

Package Information

No. Package Code Package Description Billing Unit
143857-0576-130 mL in 1 BOTTLE, DROPPER (43857-0576-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0576The 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 NAMEB ForceThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEchinacea Angustifolia, Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Tabebuia Impetiginosa, Hydrastis Canadensis, Propolis, Glandula Suprarenalis Suis, Lymph Node (Suis), Spleen (Suis), Thymus (Suis), Thyroidinum (Suis), Arsenicum Album, Belladonna, Hypericum Perforatum, Phosphorus, Botulinum, Colibacillinum Cum Natrum Muriaticum, Proteus (Vulgaris), Pseudomonas Aeruginosa, Proteus (Morgani), Salmonella Typhi Nosode, Clostridium PerfringensThe 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 DATE5/4/2021This 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 NAMEECHINACEA ANGUSTIFOLIA WHOLE; LOMATIUM DISSECTUM ROOT; MYRRH; NASTURTIUM OFFICINALE; HANDROANTHUS IMPETIGINOSUS BARK; GOLDENSEAL; PROPOLIS WAX; SUS SCROFA ADRENAL GLAND; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; SUS SCROFA THYROID; ARSENIC TRIOXIDE; ATROPA BELLADONNA; HYPERICUM PERFORATUM WHOLE; PHOSPHORUS; BOTULINUM TOXIN TYPE A; ESCHERICHIA COLI; PROTEUS VULGARIS; PSEUDOMONAS AERUGINOSA; PROTEUS MORGANII; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI; CLOSTRIDIUM PERFRINGENSThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH3; 3; 3; 3; 3; 5; 6; 8; 8; 8; 8; 8; 12; 12; 12; 12; 30; 30; 30; 30; 30; 33; 15 
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_X]/mL; [hp_X]/mL; [hp_C]/mL 

Download Record

Download this NDC record in Text format: Export

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

Download this NDC record in XML format: Export

This page was last updated on: 11/8/2021