1. Home
  2. Labeler Index
  3. King Bio Inc.
  4. NDC Product Code: 57955-3020 Alcoholism

NDC 57955-3020 Alcoholism

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-3020?
  4. Alcoholism 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.

Get all the details for National Drug Code (NDC) 57955-3020 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
57955-3020
Proprietary Name:
Alcoholism
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
11e13ea9-010b-47f0-bbab-da36c534f6a5
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
06-26-2013
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57955-3020?

The NDC code 57955-3020 is assigned by the FDA to the product Alcoholism 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 57955-3020-2 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 Alcoholism?

Uses a natural aid for: emotional and physical effects of alcohol, alcoholic tendencies or predisposition, discontent, irritability.

Which are Alcoholism 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)
  • APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z)
  • APOCYNUM CANNABINUM ROOT (UNII: 2F92409L9Z) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • ASARUM EUROPAEUM (UNII: H0876AL67A)
  • ASARUM EUROPAEUM (UNII: H0876AL67A) (Active Moiety)
  • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
  • AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
  • CAPSICUM (UNII: 00UK7646FG)
  • CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
  • CARBON DISULFIDE (UNII: S54S8B99E8)
  • CARBON DISULFIDE (UNII: S54S8B99E8) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
  • HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) (Active Moiety)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
  • LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY)
  • LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY) (Active Moiety)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
  • PAULLINIA CUPANA SEED (UNII: C21GE7524R)
  • PAULLINIA CUPANA SEED (UNII: C21GE7524R) (Active Moiety)

Which are Alcoholism 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:

* Please review the disclaimer below.

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, 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".