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  4. NDC Product Code: 69164-2001 Colloidal Iodine

NDC 69164-2001 Colloidal Iodine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69164-2001?
  4. Colloidal Iodine 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:
69164-2001
Proprietary Name:
Colloidal Iodine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jci Institute Of Medical Science
Labeler Code:
69164
Product Label ID:
9c95d6ca-407c-4b60-8ea1-9f2908a42a05
Start Marketing Date: [9]
08-27-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69164-2001-1

Package Description: 500 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 69164-2001?

The NDC code 69164-2001 is assigned by the FDA to the product Colloidal Iodine which is product labeled by Jci Institute Of Medical Science. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69164-2001-1 500 ml in 1 bottle, glass . 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 Colloidal Iodine?

It is better to dose on an empty stomachthe dosage on undiluted solution is possibly recommendeddo eat nothing within five minutes after the dosageunit dose is 30mldo take unit dose three times a day before each meal (morning, daylight, evening)keep this dose guide for a monthif effective, do change the unit dose twice a day before each meal (morning, evening)do discuss with your doctor for further dose

Which are Colloidal Iodine UNII Codes?

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

Which are Colloidal Iodine 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".