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  4. NDC Product Code: 57955-1751 Intense Anxiety

NDC 57955-1751 Intense Anxiety

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-1751?
  4. Intense Anxiety 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:
57955-1751
Proprietary Name:
Intense Anxiety
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
8080a78d-30fe-4155-817f-354131aa652b
Start Marketing Date: [9]
01-13-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57955-1751?

The NDC code 57955-1751 is assigned by the FDA to the product Intense Anxiety 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 57955-1751-2 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 Intense Anxiety?

Uses a natural aid for: anxiety attacks, anguish, apprehension, fear, despair.

Which are Intense Anxiety UNII Codes?

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

  • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • AETHUSA CYNAPIUM (UNII: M6936L953C)
  • AETHUSA CYNAPIUM (UNII: M6936L953C) (Active Moiety)
  • SILVER NITRATE (UNII: 95IT3W8JZE)
  • SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • BORAGE (UNII: PB618V0K2W)
  • BORAGE (UNII: PB618V0K2W) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3)
  • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3) (Active Moiety)
  • CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666)
  • CYTISUS SCOPARIUS FLOWERING TOP (UNII: XZC6H8R666) (Active Moiety)
  • DIGITALIS (UNII: F1T8QT9U8B)
  • DIGITALIS (UNII: F1T8QT9U8B) (Active Moiety)
  • ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H)
  • ERIODICTYON CALIFORNICUM LEAF (UNII: 2Y7TIQ135H) (Active Moiety)
  • JATROPHA CURCAS SEED (UNII: J0F5GM8LA8)
  • JATROPHA CURCAS SEED (UNII: J0F5GM8LA8) (Active Moiety)
  • PRUNUS LAUROCERASUS LEAF (UNII: F26P2D4757)
  • PRUNUS LAUROCERASUS LEAF (UNII: F26P2D4757) (Active Moiety)
  • LOLIUM TEMULENTUM TOP (UNII: GMD3D1SA75)
  • LOLIUM TEMULENTUM TOP (UNII: GMD3D1SA75) (Active Moiety)
  • HIPPOMANE MANCINELLA FRUITING LEAFY TWIG (UNII: HU6EYI2I1W)
  • HIPPOMANE MANCINELLA FRUITING LEAFY TWIG (UNII: HU6EYI2I1W) (Active Moiety)
  • HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE (UNII: IQV54TN60Y)
  • HEXAPLEX TRUNCULUS HYPOBRANCHIAL GLAND JUICE (UNII: IQV54TN60Y) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK)
  • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK) (Active Moiety)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
  • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)

Which are Intense Anxiety 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".