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  4. NDC Product Code: 43857-0588 Joint Tonic R II

NDC 43857-0588 Joint Tonic R II

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0588?
  4. Joint Tonic R II Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
43857-0588
Proprietary Name:
Joint Tonic R II
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
77afccf5-4e9c-45a1-8a6a-e686bcf22f16
Start Marketing Date: [9]
05-20-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43857-0588-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 43857-0588?

The NDC code 43857-0588 is assigned by the FDA to the product Joint Tonic R II which is product labeled by Bioactive Nutritional, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43857-0588-1 60 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Joint Tonic R II?

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.

Which are Joint Tonic R II 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 Joint Tonic R II Inactive Ingredients 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 Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".