NDC 43857-0568 Arterioforce II
Baptisia Tinctoria,Echinacea (angustifolia),Myrrha,Nasturtium Aquaticum,Phytolacca - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0568 - Arterioforce
Product Packages
NDC Code 43857-0568-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43857-0568?
What are the uses for Arterioforce II?
What are Arterioforce II Active Ingredients?
- ARNICA MONTANA WHOLE 6 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- BARIUM CARBONATE 12 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM 12 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- FENUGREEK SEED 4 [hp_X]/mL
- GOLDENSEAL 5 [hp_X]/mL
- MYRRH 4 [hp_X]/mL
- NASTURTIUM OFFICINALE 4 [hp_X]/mL - A plant genus of the family BRASSICACEAE. Nasturtium is also used as a common name for TROPAEOLUM. The common name of watercress is also used for RORIPPA & TROPAEOLUM. This is the most popular of the edible cresses, is a hardy creeping perennial plant, native to Europe but extensively naturalized elsewhere in moist places.
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- POTASSIUM IODIDE 5 [hp_X]/mL - An inorganic compound that is used as a source of iodine in thyrotoxic crisis and in the preparation of thyrotoxic patients for thyroidectomy. (From Dorland, 27th ed)
- PROPOLIS WAX 6 [hp_X]/mL
- SELENICEREUS GRANDIFLORUS STEM 6 [hp_X]/mL
Which are Arterioforce II UNII Codes?
The UNII codes for the active ingredients in this product are:
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- MYRRH (UNII: JC71GJ1F3L)
- MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676)
- NASTURTIUM OFFICINALE (UNII: YH89GMV676) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- FENUGREEK SEED (UNII: 654825W09Z)
- FENUGREEK SEED (UNII: 654825W09Z) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (Active Moiety)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
Which are Arterioforce 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[1] 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.
[2] 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.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] 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.
[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".