Procrastination
NDC 57955-2760

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 57955-2760?
  4. Procrastination 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.

Procrastination is a UNAPPROVED HOMEOPATHIC-approved product labeled by King Bio Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 57955-2760 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
57955-2760
Proprietary Name:
Procrastination
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
e76a38ab-d134-4c1d-a230-910f22a3b96b
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
06-15-2013
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 57955-2760?

The NDC code 57955-2760 is assigned by the FDA to the product Procrastination. This pharmaceutical product is labeled by King Bio Inc. 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: 57955-2760-2. 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?

Uses a natural aid for: tendencies to procrastinate, leave tasks incomplete, avoid responsibility, lose track of time.

Which are the associated UNII Codes?

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

  • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
  • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
  • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
  • ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN)
  • ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (Active Moiety)
  • CAPSICUM (UNII: 00UK7646FG)
  • CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
  • CARPINUS BETULUS FLOWERING TOP (UNII: QOI241B01F)
  • CARPINUS BETULUS FLOWERING TOP (UNII: QOI241B01F) (Active Moiety)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
  • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)
  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
  • NITROGLYCERIN (UNII: G59M7S0WS3)
  • NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
  • STRYCHNOS WALLICHIANA BARK (UNII: OQ16ZEE7O7)
  • STRYCHNOS WALLICHIANA BARK (UNII: OQ16ZEE7O7) (Active Moiety)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
  • LARIX DECIDUA FLOWERING TOP (UNII: 9UMZ642257)
  • LARIX DECIDUA FLOWERING TOP (UNII: 9UMZ642257) (Active Moiety)
  • LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY)
  • LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY) (Active Moiety)
  • MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU)
  • MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
  • OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
  • OXYTROPIS LAMBERTII TOP (UNII: 0O0H79JKAY)
  • OXYTROPIS LAMBERTII TOP (UNII: 0O0H79JKAY) (Active Moiety)
  • PICRIC ACID (UNII: A49OS0F91S)
  • PICRIC ACID (UNII: A49OS0F91S) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • SCLERANTHUS ANNUUS FLOWERING TOP (UNII: CC4B5WU2XX)
  • SCLERANTHUS ANNUUS FLOWERING TOP (UNII: CC4B5WU2XX) (Active Moiety)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
  • CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
  • STELLARIA MEDIA (UNII: 2H03479QVR)
  • STELLARIA MEDIA (UNII: 2H03479QVR) (Active Moiety)
  • SULFURIC ACID (UNII: O40UQP6WCF)
  • SULFURIC ACID (UNII: O40UQP6WCF) (Active Moiety)

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".