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  4. NDC Product Code: 58214-456 Beyond Insomnia

NDC 58214-456 Beyond Insomnia

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58214-456?
  4. Beyond Insomnia Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
58214-456
Proprietary Name:
Beyond Insomnia
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jmsp Usa Llc
Labeler Code:
58214
Product Label ID:
ddc74d7d-4a53-4050-a591-16366d1d1c8c
Start Marketing Date: [9]
06-10-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 58214-456-01

Package Description: 30 mL in 1 PACKAGE

Product Details

What is NDC 58214-456?

The NDC code 58214-456 is assigned by the FDA to the product Beyond Insomnia 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 58214-456-01 30 ml in 1 package . 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 Insomnia?

One pump spray under the tongue up to 6 times a day, or as needed

Which are Beyond Insomnia UNII Codes?

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

  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
  • COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E)
  • COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)

Which are Beyond Insomnia 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:

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Product Footnotes

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

[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".