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  4. NDC Product Code: 80746-100 Saturday Skin Hand Sanitizing Mist

NDC 80746-100 Saturday Skin Hand Sanitizing Mist

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80746-100?
  4. Saturday Skin Hand Sanitizing Mist 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:
80746-100
Proprietary Name:
Saturday Skin Hand Sanitizing Mist
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chalogy, Inc.
Labeler Code:
80746
Product Label ID:
b43dd46d-ed0e-0569-e053-2a95a90afede
Start Marketing Date: [9]
11-18-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 80746-100?

The NDC code 80746-100 is assigned by the FDA to the product Saturday Skin Hand Sanitizing Mist which is product labeled by Chalogy, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80746-100-01 30 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 Saturday Skin Hand Sanitizing Mist?

Hand Sanitizer to help reduce bacteria that potentially can cause disease

Which are Saturday Skin Hand Sanitizing Mist UNII Codes?

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

Which are Saturday Skin Hand Sanitizing Mist 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".