NDC 43857-0469 Psoriaforce

Baptisia Tinctoria, Berberis Vulgaris, Echinacea (angustifolia), Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Rhamnus Purshiana, Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Hydrastis Canadensis, Arsenicum Iodatum, Calcarea Carbonica, Clematis Erecta, Graphites, Kali Muriaticum, Kali Sulphuricum, Mezereum, Petroleum, Sepia

NDC Product Code 43857-0469

NDC Code: 43857-0469

Proprietary Name: Psoriaforce 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, Berberis Vulgaris, Echinacea (angustifolia), Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Rhamnus Purshiana, Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Hydrastis Canadensis, Arsenicum Iodatum, Calcarea Carbonica, Clematis Erecta, Graphites, Kali Muriaticum, Kali Sulphuricum, Mezereum, Petroleum, Sepia 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.

NDC Code Structure

  • 43857 - Bioactive Nutritional, Inc.
    • 43857-0469 - Psoriaforce

NDC 43857-0469-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Psoriaforce with NDC 43857-0469 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Psoriaforce is baptisia tinctoria, berberis vulgaris, echinacea (angustifolia), glycyrrhiza glabra, lappa major, rhamnus frangula, rhamnus purshiana, trifolium pratense, xanthoxylum fraxineum, phytolacca decandra, hydrastis canadensis, arsenicum iodatum, calcarea carbonica, clematis erecta, graphites, kali muriaticum, kali sulphuricum, mezereum, petroleum, sepia. 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.

Psoriaforce 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
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 3 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • FRANGULA ALNUS BARK 3 [hp_X]/mL
  • FRANGULA PURSHIANA BARK 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • ARSENIC TRIIODIDE 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • CLEMATIS RECTA FLOWERING TOP 12 [hp_X]/mL
  • GRAPHITE 12 [hp_X]/mL
  • POTASSIUM CHLORIDE 12 [hp_X]/mL
  • POTASSIUM SULFATE 12 [hp_X]/mL
  • DAPHNE MEZEREUM BARK 12 [hp_X]/mL
  • KEROSENE 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 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.

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: 02-23-2018 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: 12-31-2019 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.

Psoriaforce Product Label Images

Psoriaforce 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, Berberis Vulgaris 3X, Echinacea (Angustifolia) 3X, Glycyrrhiza Glabra 3X, Lappa Major 3X, Rhamnus Frangula 3X, Rhamnus Purshiana 3X, Trifolium Pratense 3X, Xanthoxylum Fraxineum 3X, Phytolacca Decandra 4X, Hydrastis Canadensis 5X, Arsenicum Iodatum 12X, Calcarea Carbonica 12X, Clematis Erecta 12X, Graphites 12X, Kali Muriaticum 12X, Kali Sulphuricum 12X, Mezereum 12X, Petroleum 12X, Sepia 12X.

Indications:

For temporary relief of unhealthy irritated or broken skin, itching, burning, swelling of skin, dry rough, scaly skin and eruptions on scalp and bends of joints with itching.

For temporary relief of unhealthy irritated or broken skin, itching, burning, swelling of skin, dry rough, scaly skin and eruptions on scalp and bends of joints with itching.

Warnings:

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

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical attention 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 NutritionalPSORIAFORCEHOMEOPATHIC1 FL OZ (30 ml)

* Please review the disclaimer below.

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