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NDC 63479-0214 B14 Bronchotox

Belladonna,Blatta Orientalis,Coccus Cacti,Corallium Rubrum,Cuprum Metallicum,Drosera - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0214?
  4. B14 Bronchotox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Get all the details for National Drug Code (NDC) 63479-0214 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
63479-0214
Proprietary Name:
B14 Bronchotox
Non-Proprietary Name: [1]
Belladonna, Blatta Orientalis, Coccus Cacti, Corallium Rubrum, Cuprum Metallicum, Drosera Rotundifolia, Echinacea Angustifolia, Hedera Helix, Hydrastis Canadensis, Ipecacuanha, Kali Nitricum, Lac Vaccinum, Lobelia Inflata, Passiflora Incarnata, Pertussinum, Sambucus Nigra, Thymus Serpyllum, Valeriana Officinalis
Substance Name: [2]
Atropa Belladonna; Blatta Orientalis; Copper; Corallium Rubrum Exoskeleton; Cow Milk; Drosera Rotundifolia; Echinacea Angustifolia; Goldenseal; Hedera Helix Flowering Twig; Human Sputum, Bordetella Pertussis Infected; Ipecac; Lobelia Inflata; Passiflora Incarnata Flowering Top; Potassium Nitrate; Protortonia Cacti; Sambucus Nigra Flowering Top; Thymus Serpyllum; Valerian
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
Sublingual - Administration beneath the tongue.
Labeler Name: [5]
Apex Energetics Inc.
Labeler Code:
63479
Product Label ID:
beeaca49-a683-7e57-e053-2995a90ac04f
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
11-01-1994
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
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Product Details

What is NDC 63479-0214?

The NDC code 63479-0214 is assigned by the FDA to the product B14 Bronchotox which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of B14 Bronchotox is belladonna, blatta orientalis, coccus cacti, corallium rubrum, cuprum metallicum, drosera rotundifolia, echinacea angustifolia, hedera helix, hydrastis canadensis, ipecacuanha, kali nitricum, lac vaccinum, lobelia inflata, passiflora incarnata, pertussinum, sambucus nigra, thymus serpyllum, valeriana officinalis. The product's dosage form is solution/ drops and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 63479-0214-1 30 ml in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for B14 Bronchotox?

Adults & children ages 12 years and over: Take 10 drops under the tongue 3-4 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

What are B14 Bronchotox Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Which are B14 Bronchotox UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are B14 Bronchotox Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes for B14 Bronchotox?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product Footnotes

[1] 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.

[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

[3] 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.

[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".