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  4. NDC Product Code: 79617-200 Cloh Living Hand Sanitizer

NDC 79617-200 Cloh Living Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 79617-200?
  5. Cloh Living Hand Sanitizer Uses
  6. Active Ingredients UNII Codes
  7. 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:
79617-200
Proprietary Name:
Cloh Living Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Spacelink Corporation
Labeler Code:
79617
Product Label ID:
e1aae972-fb3a-4670-e053-2995a90abbd5
Start Marketing Date: [9]
06-17-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Code Structure Chart

Product Details

What is NDC 79617-200?

The NDC code 79617-200 is assigned by the FDA to the product Cloh Living Hand Sanitizer which is product labeled by Spacelink Corporation. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 79617-200-01 500 ml in 1 bottle, spray , 79617-200-02 60 ml in 1 bottle, spray , 79617-200-03 1000 ml in 1 bottle , 79617-200-04 4000 ml in 1 bottle , 79617-200-05 20000 ml in 1 bottle . 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 Cloh Living Hand Sanitizer?

Place enough product on hands to cover all surfaces. Rub hands together until dry.For children under 6, use only under adult supervision.Not recommended for infants.

Which are Cloh Living Hand Sanitizer UNII Codes?

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

Which are Cloh Living 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".