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  4. NDC Product Code: 57955-5152 Fears And Phobias

NDC 57955-5152 Fears And Phobias

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-5152?
  4. Fears And Phobias 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:
57955-5152
Proprietary Name:
Fears And Phobias
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
b142b81a-6ff8-4dfc-b7fb-37bd7d055fa9
Start Marketing Date: [9]
10-11-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57955-5152?

The NDC code 57955-5152 is assigned by the FDA to the product Fears And Phobias 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 57955-5152-2 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 Fears And Phobias?

Uses a natural aid to help relieve fears related to people, places, situations or things, including: something happening, being alone, imaginary things, losing reasoning, crowds, public places, death, evil or ghosts, misfortune or poverty, dread of work, anxiety, despair and suspiciousness.Reference image fears and phobias.jpg

Which are Fears And Phobias UNII Codes?

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

  • ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88)
  • ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88) (Active Moiety)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • SILVER NITRATE (UNII: 95IT3W8JZE)
  • SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO) (Active Moiety)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
  • CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U)
  • ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • POTASSIUM ARSENITE ANHYDROUS (UNII: BM2U42PAKI)
  • POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
  • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
  • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
  • DATURA STRAMONIUM (UNII: G6W4F0V8Z3)
  • DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (Active Moiety)

Which are Fears And Phobias 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".