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  4. NDC Product Code: 80891-234 Soft Foam Hand Sanitizer

NDC 80891-234 Soft Foam Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80891-234?
  4. Soft Foam 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:
80891-234
Proprietary Name:
Soft Foam Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Freedom Technologies Llc
Labeler Code:
80891
Product Label ID:
b2990d1f-df96-614f-e053-2a95a90a7539
Start Marketing Date: [9]
10-01-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 80891-234?

The NDC code 80891-234 is assigned by the FDA to the product Soft Foam Hand Sanitizer which is product labeled by Freedom Technologies Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80891-234-02 1 bottle in 1 box / 3780 mg in 1 bottle (80891-234-01). 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 Soft Foam Hand Sanitizer?

Antibacertial foaming hand cleaner. Use in daycare, nursing homes, restaurants, doctors offices, dental offices, schools and clinics

Which are Soft Foam Hand Sanitizer UNII Codes?

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

Which are Soft Foam 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".