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  4. NDC Product Code: 57955-0921 Eczema Symptom Relief

NDC 57955-0921 Eczema Symptom Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-0921?
  4. Eczema Symptom Relief 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:
57955-0921
Proprietary Name:
Eczema Symptom Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
a4751819-d243-4c0d-b381-072070c141a5
Start Marketing Date: [9]
03-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 57955-0921?

The NDC code 57955-0921 is assigned by the FDA to the product Eczema Symptom Relief 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 57955-0921-3 1 tube in 1 carton / 85 g in 1 tube. 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 Eczema Symptom Relief?

Uses for temporary relief of eczema: •redness •intense itching •allergic skin eruptions •dry or moist eruptions •thickened, crusty, scaly skin •inflamed skin •general unhealthy skin

Which are Eczema Symptom Relief UNII Codes?

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

  • CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR)
  • CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR) (Active Moiety)
  • GOLDENSEAL (UNII: ZW3Z11D0JV)
  • GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
  • CENTELLA ASIATICA (UNII: 7M867G6T1U)
  • CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
  • ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
  • ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
  • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
  • RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
  • TARAXACUM OFFICINALE (UNII: 39981FM375)
  • TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)

Which are Eczema Symptom Relief 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".