Joint Tonic R Liquid
NDC 43857-0588

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0588?
  4. Joint Tonic R II Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

Joint Tonic R (harpagophytum procumbens, salix alba, colchicum autumnale, pinus sylvestris, symphytum officinale, aconitum napellus, arnica montana, gelsemium sempervirens, iris versicolor, ledum palustre, lespedeza capitata, rhus tox, secale cornutum, spigelia anthelmia, spiraea ulmaria, tartaricum acidum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bioactive Nutritional, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43857-0588 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43857-0588
Proprietary Name:
Joint Tonic R II
Non-Proprietary Name: [1]
Harpagophytum Procumbens, Salix Alba, Colchicum Autumnale, Pinus Sylvestris, Symphytum Officinale, Aconitum Napellus, Arnica Montana, Gelsemium Sempervirens, Iris Versicolor, Ledum Palustre, Lespedeza Capitata, Rhus Tox, Secale Cornutum, Spigelia Anthelmia, Spiraea Ulmaria, Tartaricum Acidum
Substance Name: [2]
Aconitum Napellus Whole; Arnica Montana Whole; Claviceps Purpurea Sclerotium; Colchicum Autumnale Bulb; Comfrey Root; Filipendula Ulmaria Root; Gelsemium Sempervirens Root; Harpagophytum Procumbens Root; Iris Versicolor Root; Lespedeza Capitata Flowering Top; Pinus Sylvestris Leafy Twig; Rhododendron Tomentosum Leafy Twig; Salix Alba Bark; Spigelia Anthelmia Whole; Tartaric Acid; Toxicodendron Pubescens Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
77afccf5-4e9c-45a1-8a6a-e686bcf22f16
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-20-2021
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43857-0588?

The NDC code 43857-0588 is assigned by the FDA to the product Joint Tonic R II. It is commonly known by its generic name, harpagophytum procumbens, salix alba, colchicum autumnale, pinus sylvestris, symphytum officinale, aconitum napellus, arnica montana, gelsemium sempervirens, iris versicolor, ledum palustre, lespedeza capitata, rhus tox, secale cornutum, spigelia anthelmia, spiraea ulmaria, tartaricum acidum. This pharmaceutical product is labeled by Bioactive Nutritional, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43857-0588-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

For temporary relief of symptoms due to swelling of wrist, pain and swelling of knees, joints red and swollen, and hot pain in the big toe. For temporary relief of symptoms due to swelling of wrist, pain and swelling of knees, joints red and swollen, and hot pain in the big toe.

What are Active Ingredients of this product?

An 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.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
  • HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89) (Active Moiety)
  • SALIX ALBA BARK (UNII: 205MXS71H7)
  • SALIX ALBA BARK (UNII: 205MXS71H7) (Active Moiety)
  • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
  • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73)
  • PINUS SYLVESTRIS LEAFY TWIG (UNII: Q1RGP4UB73) (Active Moiety)
  • COMFREY ROOT (UNII: M9VVZ08EKQ)
  • COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
  • IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
  • RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
  • LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
  • LESPEDEZA CAPITATA FLOWERING TOP (UNII: F930LFZ4LF)
  • LESPEDEZA CAPITATA FLOWERING TOP (UNII: F930LFZ4LF) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
  • SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE)
  • SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
  • FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)
  • FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (Active Moiety)
  • TARTARIC ACID (UNII: W4888I119H)
  • TARTARIC ACID (UNII: W4888I119H) (Active Moiety)

Which are the Inactive Ingredients associated UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An 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.
What kind of product is this? Indicates 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".