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  4. NDC Product Code: 43857-0621 Jointforce R-hp

NDC 43857-0621 Jointforce R-hp

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0621?
  4. Jointforce R-hp 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:
43857-0621
Proprietary Name:
Jointforce R-hp
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
9d243d5d-af08-470f-b3ec-b733bb91d1a2
Start Marketing Date: [9]
02-03-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43857-0621-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 43857-0621?

The NDC code 43857-0621 is assigned by the FDA to the product Jointforce R-hp 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 43857-0621-1 30 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 Jointforce R-hp?

For temporary relief of symptoms such as aches, pains, fever, and swelling due to inflammation of the connective tissue surrounding the joints; weak and numb feeling limbs; gouty pains in foot and painful soles. For temporary relief of symptoms such as aches, pains, fever, and swelling due to inflammation of the connective tissue surrounding the joints; weak and numb feeling limbs; gouty pains in foot and painful soles.

Which are Jointforce R-hp UNII Codes?

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

  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
  • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
  • KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
  • KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
  • LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
  • LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U)
  • RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)

Which are Jointforce R-hp 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".