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  5. NDC Package Code: 43857-0469-1 Psoriaforce

NDC Package 43857-0469-1 Psoriaforce

Baptisia Tinctoria,Berberis Vulgaris,Echinacea (angustifolia),Glycyrrhiza Glabra,Lappa - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
43857-0469-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43857-0469
Proprietary Name:
Psoriaforce
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
Substance Name:
Arctium Lappa Root; Arsenic Triiodide; Baptisia Tinctoria Root; Berberis Vulgaris Root Bark; Clematis Recta Flowering Top; Daphne Mezereum Bark; Echinacea Angustifolia; Frangula Alnus Bark; Frangula Purshiana Bark; Glycyrrhiza Glabra; Goldenseal; Graphite; Kerosene; Oyster Shell Calcium Carbonate, Crude; Phytolacca Americana Root; Potassium Chloride; Potassium Sulfate; Sepia Officinalis Juice; Trifolium Pratense Flower; Zanthoxylum Americanum Bark
Usage Information:
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.
11-Digit NDC Billing Format:
43857046901
Product Type:
Human Otc Drug
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.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • ARSENIC TRIIODIDE 12 [hp_X]/mL
  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • CLEMATIS RECTA FLOWERING TOP 12 [hp_X]/mL
  • DAPHNE MEZEREUM BARK 12 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • FRANGULA ALNUS BARK 3 [hp_X]/mL
  • FRANGULA PURSHIANA BARK 3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 3 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • GRAPHITE 12 [hp_X]/mL
  • KEROSENE 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • POTASSIUM CHLORIDE 12 [hp_X]/mL
  • POTASSIUM SULFATE 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    02-23-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 43857-0469-1?

    The NDC Packaged Code 43857-0469-1 is assigned to a package of 30 ml in 1 bottle, dropper of Psoriaforce, a human over the counter drug labeled by Bioactive Nutritional, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 43857-0469 included in the NDC Directory?

    Yes, Psoriaforce with product code 43857-0469 is active and included in the NDC Directory. The product was first marketed by Bioactive Nutritional, Inc. on February 23, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 43857-0469-1?

    The 11-digit format is 43857046901. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-143857-0469-15-4-243857-0469-01