Beyond Nicotine Kit
NDC 58214-100

View dosage, usage, ingredients, routes, and UNII mappings.
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.

Beyond Nicotine Kit is a UNAPPROVED HOMEOPATHIC-approved product labeled by Jmsp Usa Llc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a red product. This product entry covers the primary NDC 58214-100 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
58214-100
Proprietary Name:
Beyond Nicotine Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

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.

Marketing Timeline

Start Marketing Date: [9]
04-17-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I

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. This pharmaceutical product is labeled by Jmsp Usa Llc and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 58214-100-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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:

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Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".