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  5. NDC Package Code: 43857-0528-1 Envirotox

NDC Package 43857-0528-1 Envirotox

Triticum Aestivum,Berberis Vulgaris,Lappa Major,Rhamnus Cathartica,Rhamnus - 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:
43857-0528-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43857-0528
Proprietary Name:
Envirotox
Non-Proprietary Name:
Triticum Aestivum, Berberis Vulgaris, Lappa Major, Rhamnus Cathartica, Rhamnus Purshiana, Phytolacca Decandra, Glycyrrhiza Glabra, Stillingia Sylvatica, Trifolium Pratense, Xanthoxylum Fraxineum, Acetonum Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Belladonna, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum
Substance Name:
Acetone; Ammonium Chloride; Arctium Lappa Root; Atropa Belladonna Whole; Benzene; Berberis Vulgaris Root Bark; Frangula Purshiana Bark; Glycyrrhiza Glabra; Lycopodium Clavatum Spore; Nitric Acid; Phosphoric Acid; Phytolacca Americana Root; Propylene Glycol; Rhamnus Cathartica Fruit; Sodium Lauryl Sulfate; Sodium Tripolyphosphate; Stillingia Sylvatica Root; Strychnos Nux-vomica Seed; Trifolium Pratense Flower; Triticum Aestivum Whole; Turpentine Oil; Zanthoxylum Americanum Bark
Usage Information:
For temporary relief of head congestion & general exhaustion as a consequence of exposure to smog, dust, or industrial agents. For temporary relief of head congestion & general exhaustion as a consequence of exposure to smog, dust, or industrial agents.
11-Digit NDC Billing Format:
43857052801
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):
  • ACETONE 9 [hp_X]/mL
  • AMMONIUM CHLORIDE 9 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • ATROPA BELLADONNA WHOLE 12 [hp_X]/mL
  • BENZENE 9 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • FRANGULA PURSHIANA BARK 3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 6 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • PROPYLENE GLYCOL 9 [hp_X]/mL
  • RHAMNUS CATHARTICA FRUIT 3 [hp_X]/mL
  • SODIUM LAURYL SULFATE 9 [hp_X]/mL
  • SODIUM TRIPOLYPHOSPHATE 9 [hp_X]/mL
  • STILLINGIA SYLVATICA ROOT 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 6 [hp_X]/mL
  • TRITICUM AESTIVUM WHOLE 1 [hp_X]/mL
  • TURPENTINE OIL 9 [hp_X]/mL
  • ZANTHOXYLUM AMERICANUM BARK 6 [hp_X]/mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    12-23-2019
    End Marketing Date:
    01-07-2025
    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 43857-0528-1?

    The NDC Packaged Code 43857-0528-1 is assigned to a package of 30 ml in 1 bottle, dropper of Envirotox, 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 43857-0528 included in the NDC Directory?

    Yes, Envirotox with product code 43857-0528 is active and included in the NDC Directory. The product was first marketed by Bioactive Nutritional, Inc. on December 23, 2019.

    What is the 11-digit format for NDC 43857-0528-1?

    The 11-digit format is 43857052801. 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
    5-4-143857-0528-15-4-243857-0528-01