NDC 43857-0396 Arterioforce II

Baptisia Tinctoria, Echinacea (angustifolia), Phytolacca Decandra, Myrrha, Nasturtium Aquaticum, Trigonella Foenum-graecum, Hydrastis Canadensis, Kali Iodatum, Arnica Montana, Cactus Grandiflorus, Propolis, Baryta Carbonica, Conium Maculatum, Secale Cornutum

NDC Product Code 43857-0396

NDC CODE: 43857-0396

Proprietary Name: Arterioforce II What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Baptisia Tinctoria, Echinacea (angustifolia), Phytolacca Decandra, Myrrha, Nasturtium Aquaticum, Trigonella Foenum-graecum, Hydrastis Canadensis, Kali Iodatum, Arnica Montana, Cactus Grandiflorus, Propolis, Baryta Carbonica, Conium Maculatum, Secale Cornutum 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Potassium iodide is used to loosen and break up mucus in the airways. This helps you cough up the mucus so you can breathe more easily if you have long-term lung problems (e.g., asthma, chronic bronchitis, emphysema). This medication is known as an expectorant. Potassium iodide is also used along with antithyroid medicines to prepare the thyroid gland for surgical removal, to treat certain overactive thyroid conditions (hyperthyroidism), and to protect the thyroid in a radiation exposure emergency. It works by shrinking the size of the thyroid gland and decreasing the amount of thyroid hormones produced. In a radiation emergency, potassium iodide blocks only the thyroid from absorbing radioactive iodine, protecting it from damage and reducing the risk of thyroid cancer. Use this medication along with other emergency measures that will be recommended to you by public health and safety officials (e.g., finding safe shelter, evacuation, controlling food supply).

NDC Code Structure

  • 43857 - Bioactive Nutritional, Inc.

NDC 43857-0396-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Arterioforce II with NDC 43857-0396 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Arterioforce II is baptisia tinctoria, echinacea (angustifolia), phytolacca decandra, myrrha, nasturtium aquaticum, trigonella foenum-graecum, hydrastis canadensis, kali iodatum, arnica montana, cactus grandiflorus, propolis, baryta carbonica, conium maculatum, secale cornutum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, Inc.

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.

Product Type: Human Otc Drug 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.

Arterioforce II Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • MYRRH 4 [hp_X]/mL
  • NASTURTIUM OFFICINALE 4 [hp_X]/mL
  • FENUGREEK SEED 4 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • POTASSIUM IODIDE 5 [hp_X]/mL
  • ARNICA MONTANA 6 [hp_X]/mL
  • SELENICEREUS GRANDIFLORUS STEM 6 [hp_X]/mL
  • PROPOLIS WAX 6 [hp_X]/mL
  • BARIUM CARBONATE 12 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
  • CLAVICEPS PURPUREA SCLEROTIUM 12 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Bioactive Nutritional, Inc.
Labeler Code: 43857
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 05-31-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Arterioforce II Product Label Images

Arterioforce II Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X, Phytolacca Decandra 3X, Myrrha 4X, Nasturtium Aquaticum 4X, Trigonella Foenum-Graecum 4X, Hydrastis Canadensis 5X, Kali Iodatum 5X, Arnica Montana 6X, Cactus Grandiflorus 6X, Propolis 6X, Baryta Carbonica 12X, Conium Maculatum 12X, Secale Cornutum 12X.

Indications:

For temporary relief of swollen extremities that feel bruised and sore, cold clammy feet, mild burning pains in lower limbs, leg cramps.

For temporary relief of swollen extremities that feel bruised and sore, cold clammy feet, mild burning pains in lower limbs, leg cramps.

Warnings:

If pregnant or breast-feeding, ask a health care professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in cool, dry place.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Distributed by:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935bioactivenutritional.com

Package Label Display:

BIOActive NutritionalARTERIOFORCE IIHOMEOPATHIC1 FL OZ (30 ml)

* Please review the disclaimer below.