NDC 57955-2331 Extravagant

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
57955-2331
Proprietary Name:
Extravagant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
57955
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
04-22-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 57955-2331?

The NDC code 57955-2331 is assigned by the FDA to the product Extravagant which is product labeled by King Bio Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57955-2331-2 59 ml in 1 bottle, spray . 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 Extravagant?

Uses for temporary relief of tendencies to: shop habitually, spend excessively, strive to live beyond one's means, dress and act extravagantly, extreme eccentric behavior.

Which are Extravagant UNII Codes?

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

  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
  • CERATOSTIGMA WILLMOTTIANUM FLOWER (UNII: TP69J995TW)
  • CERATOSTIGMA WILLMOTTIANUM FLOWER (UNII: TP69J995TW) (Active Moiety)
  • CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
  • CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
  • CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
  • TUBOCURARINE CHLORIDE (UNII: 900961Z8VR)
  • TUBOCURARINE (UNII: W9YXS298BM) (Active Moiety)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
  • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
  • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
  • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
  • PALLADIUM (UNII: 5TWQ1V240M)
  • PALLADIUM (UNII: 5TWQ1V240M) (Active Moiety)
  • PINUS SYLVESTRIS FLOWERING TOP (UNII: 2HEM73YI9I)
  • PINUS SYLVESTRIS FLOWERING TOP (UNII: 2HEM73YI9I) (Active Moiety)
  • RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
  • RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M) (Active Moiety)
  • SAGE (UNII: 065C5D077J)
  • SAGE (UNII: 065C5D077J) (Active Moiety)
  • VERBASCUM THAPSUS (UNII: C9TD27U172)
  • VERBASCUM THAPSUS (UNII: C9TD27U172) (Active Moiety)

Which are Extravagant 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.

[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 ("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".