NDC 43857-0533 Pneumotox

Triticum Aestivum, Alfalfa, Arnica Montana, Asclepias Tuberosa, Chamomilla, Echinacea (angustifolia), Eucalyptus Globulus, Fucus Vesiculosus, Hordeum Vulgare, Iodium, Nasturtium Aquaticum, Plantago Major, Raphanus Sativus, Trifolium Pratense, Trigonella Foenum-graecum, Symphytum Officinale, Lung (suis), Oryza Sativa, Silicea, Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Arsenicum Album, Natrum Muriaticum, Nitricum Acidum,

NDC Product Code 43857-0533

NDC Code: 43857-0533

Proprietary Name: Pneumotox 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: Triticum Aestivum, Alfalfa, Arnica Montana, Asclepias Tuberosa, Chamomilla, Echinacea (angustifolia), Eucalyptus Globulus, Fucus Vesiculosus, Hordeum Vulgare, Iodium, Nasturtium Aquaticum, Plantago Major, Raphanus Sativus, Trifolium Pratense, Trigonella Foenum-graecum, Symphytum Officinale, Lung (suis), Oryza Sativa, Silicea, Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Arsenicum Album, Natrum Muriaticum, Nitricum Acidum, 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.

NDC 43857-0533-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Pneumotox with NDC 43857-0533 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Pneumotox is triticum aestivum, alfalfa, arnica montana, asclepias tuberosa, chamomilla, echinacea (angustifolia), eucalyptus globulus, fucus vesiculosus, hordeum vulgare, iodium, nasturtium aquaticum, plantago major, raphanus sativus, trifolium pratense, trigonella foenum-graecum, symphytum officinale, lung (suis), oryza sativa, silicea, acetone, sodium tripolyphosphate, propylene glycol, benzinum, ammonium muriaticum, sodium lauryl sulfate, terebinthina, arsenicum album, natrum muriaticum, nitricum acidum, . 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.

Pneumotox 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.

  • TRITICUM AESTIVUM WHOLE 1 [hp_X]/mL
  • ALFALFA 3 [hp_X]/mL
  • ARNICA MONTANA 3 [hp_X]/mL
  • ASCLEPIAS TUBEROSA ROOT 3 [hp_X]/mL
  • MATRICARIA RECUTITA 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • EUCALYPTUS GLOBULUS LEAF 3 [hp_X]/mL
  • FUCUS VESICULOSUS 3 [hp_X]/mL
  • HORDEUM VULGARE TOP 3 [hp_X]/mL
  • IODINE 3 [hp_X]/mL
  • NASTURTIUM OFFICINALE 3 [hp_X]/mL
  • PLANTAGO MAJOR 3 [hp_X]/mL
  • RAPHANUS SATIVUS 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • TRIGONELLA FOENUM-GRAECUM WHOLE 3 [hp_X]/mL
  • SYMPHYTUM OFFICINALE WHOLE 6 [hp_X]/mL
  • SUS SCROFA LUNG 8 [hp_X]/mL
  • ORYZA SATIVA WHOLE 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • ACETONE 9 [hp_X]/mL
  • SODIUM TRIPOLYPHOSPHATE 9 [hp_X]/mL
  • PROPYLENE GLYCOL 9 [hp_X]/mL
  • BENZENE 9 [hp_X]/mL
  • AMMONIUM CHLORIDE 9 [hp_X]/mL
  • SODIUM LAURYL SULFATE 9 [hp_X]/mL
  • TURPENTINE OIL 9 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • SODIUM CHLORIDE 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • OENANTHE AQUATICA FRUIT 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • ANEMONE PRATENSIS 12 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL

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: 10-02-2019 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.

Pneumotox Product Label Images