44911-0743 NDC - JOINTOX BB (BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, PHYTOLACCA DECANDRA, BORRELIA BURGDORFERI NOSODE, BABESIA MICROTI, EHRLICHIA NOSODE (CANINE), HEPATITIS B NOSODE, MENINGOCOCCUS NOSODE, ACONITUM NAPELLUS, ARSENICUM ALBUM, BRYONIA (ALBA), CHELIDONIUM MAJUS, COLCHICUM AUTUMNALE, KALMIA LATIFOLIA, LEDUM PALUSTRE, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, PHOSPHORUS, RHUS TOX)

Drug Information

  • Product NDC: 44911-0743
  • Proprietary Name: Jointox BB
  • Non Proprietary Name: Baptisia Tinctoria, Echinacea (Angustifolia), Hydrastis Canadensis, Phytolacca Decandra, Borrelia Burgdorferi Nosode, Babesia Microti, Ehrlichia Nosode (Canine), Hepatitis B Nosode, Meningococcus Nosode, Aconitum Napellus, Arsenicum Album, Bryonia (Alba), Chelidonium Majus, Colchicum Autumnale, Kalmia Latifolia, Ledum Palustre, Lycopodium Clavatum, Mercurius Vivus, Phosphorus, Rhus Tox
  • Active Ingredient(s): 30 [hp_C]/mL ACONITUM NAPELLUS WHOLE; 30 [hp_C]/mL ARSENIC TRIOXIDE; 20 [hp_X]/mL BABESIA MICROTI; 3 [hp_X]/mL BAPTISIA TINCTORIA ROOT; 12 [hp_X]/mL BORRELIA BURGDORFERI; 30 [hp_C]/mL BRYONIA ALBA ROOT; 30 [hp_C]/mL CHELIDONIUM MAJUS WHOLE; 30 [hp_C]/mL COLCHICUM AUTUMNALE BULB; 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 20 [hp_X]/mL EHRLICHIA CANIS; 6 [hp_X]/mL GOLDENSEAL; 30 [hp_X]/mL HEPATITIS B VIRUS; 30 [hp_C]/mL KALMIA LATIFOLIA LEAF; 30 [hp_C]/mL LYCOPODIUM CLAVATUM SPORE; 30 [hp_C]/mL MERCURY; 30 [hp_X]/mL NEISSERIA MENINGITIDIS; 30 [hp_C]/mL PHOSPHORUS; 6 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 30 [hp_C]/mL RHODODENDRON TOMENTOSUM LEAFY TWIG; 30 [hp_C]/mL TOXICODENDRON PUBESCENS LEAF
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID

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:1/5/2026

Package Information

No. Package Code Package Description Billing Unit
144911-0743-160 mL in 1 BOTTLE, DROPPER (44911-0743-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0743The 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 NAMEJointox BBThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBaptisia Tinctoria, Echinacea (Angustifolia), Hydrastis Canadensis, Phytolacca Decandra, Borrelia Burgdorferi Nosode, Babesia Microti, Ehrlichia Nosode (Canine), Hepatitis B Nosode, Meningococcus Nosode, Aconitum Napellus, Arsenicum Album, Bryonia (Alba), Chelidonium Majus, Colchicum Autumnale, Kalmia Latifolia, Ledum Palustre, Lycopodium Clavatum, Mercurius Vivus, Phosphorus, 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 DATE1/5/2026This 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 NAMEEnergique, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS WHOLE; ARSENIC TRIOXIDE; BABESIA MICROTI; BAPTISIA TINCTORIA ROOT; BORRELIA BURGDORFERI; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS WHOLE; COLCHICUM AUTUMNALE BULB; ECHINACEA ANGUSTIFOLIA WHOLE; EHRLICHIA CANIS; GOLDENSEAL; HEPATITIS B VIRUS; KALMIA LATIFOLIA LEAF; LYCOPODIUM CLAVATUM SPORE; MERCURY; NEISSERIA MENINGITIDIS; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; RHODODENDRON TOMENTOSUM LEAFY TWIG; TOXICODENDRON PUBESCENS LEAFAn 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; 20; 3; 12; 30; 30; 30; 3; 20; 6; 30; 30; 30; 30; 30; 30; 6; 30; 30 
ACTIVE INGRED UNIT[hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL 

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

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