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  4. NDC Product Code: 57955-8020 Candida High Potency 9

NDC 57955-8020 Candida High Potency 9

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-8020?
  4. Candida High Potency 9 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:
57955-8020
Proprietary Name:
Candida High Potency 9
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
5735e63c-6370-4a72-a217-0d9feacffba3
Start Marketing Date: [9]
01-30-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 57955-8020?

The NDC code 57955-8020 is assigned by the FDA to the product Candida High Potency 9 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 57955-8020-8 1 bottle, spray in 1 box / 236 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 Candida High Potency 9?

Uses:Temporarily relieves symptoms due to overgrowth of Candida albicans yeast: yeast infections, thrush, nail fungus, constipation, headache, nausea, itchy skin, fatigue, diarrhea, flatulence, forgetfulness, sleeplessness, cravings. As per various homeopathic Materia Medicas.Referenced image of carton.jpg

Which are Candida High Potency 9 UNII Codes?

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

Which are Candida High Potency 9 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".