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  4. NDC Product Code: 78923-001 Sani-kure Extra Strength Hand Sanitizer

NDC 78923-001 Sani-kure Extra Strength Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78923-001?
  4. Sani-kure Extra Strength Hand Sanitizer 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:
78923-001
Proprietary Name:
Sani-kure Extra Strength Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kolorcure Corporation
Labeler Code:
78923
Product Label ID:
a7c04185-d309-931b-e053-2a95a90ac783
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 78923-001?

The NDC code 78923-001 is assigned by the FDA to the product Sani-kure Extra Strength Hand Sanitizer which is product labeled by Kolorcure Corporation. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 78923-001-02 59 ml in 1 bottle, spray , 78923-001-04 118 ml in 1 bottle, spray , 78923-001-08 236 ml in 1 bottle, spray , 78923-001-32 946 ml in 1 bottle, spray , 78923-001-38 3800 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 Sani-kure Extra Strength Hand Sanitizer?

Place enough product in your palm to cover hands. Rub hands together until dry.Children under 6 years of age should be supervised when using Sani-Kure.

Which are Sani-kure Extra Strength Hand Sanitizer UNII Codes?

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

Which are Sani-kure Extra Strength Hand Sanitizer 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".