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  4. NDC Product Code: 58214-100 Beyond Nicotine Kit

NDC 58214-100 Beyond Nicotine Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58214-100?
  5. Beyond Nicotine Kit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Get all the details for National Drug Code (NDC) 58214-100 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:
58214-100
Proprietary Name:
Beyond Nicotine Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jmsp Usa Llc
Labeler Code:
58214
Product Label ID:
cb60abca-aa8c-47fe-8d28-2ad836b40449
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
04-17-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
GREEN (C48329)
Shape:
ROUND (C48348)
Size(s):
7 MM
10 MM
Score:
1
2

Code Structure Chart

Product Details

What is NDC 58214-100?

The NDC code 58214-100 is assigned by the FDA to the product Beyond Nicotine Kit which is product labeled by Jmsp Usa Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58214-100-01 1 kit in 1 kit * 60 tablet, chewable in 1 pouch (58214-099-06) * 200 tablet, chewable in 1 pouch (58214-098-20). 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 Beyond Nicotine Kit?

Anti-crave pills (each pill contains: Caladium Seguinum 9C HPUS1, Kali Sulph 6x HPUS, Plantago Major 9C HPUS2, Nicotiana Tabacum 9C HPUS3)Take a red Anti-crave pill and dissolve under the tongue at intervals through-out the day when you would normally have a cigarette or when craving pangs are intense, you can take up to 20 pills per day. After the initial 5 days, reduce the frequency to around 10 pills a day.Detox tablets (each tablet contains: Calc Sulph 6x HPUS, Lobelia Inflata 9C HPUS4, Sambucus Nigra 9C HPUS5, and Staphysagria Delphinium 9C HPUS6) Take two green Detox tablets each morning and two each evening for a fifteen day period.

Which are Beyond Nicotine Kit UNII Codes?

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

Which are Beyond Nicotine Kit 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:

* Please review the disclaimer below.

Product Footnotes

[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".