1. Home
  2. Labeler Index
  3. Porter Aerospace, Llc
  4. NDC Product Code: 79211-218 Sanihands

NDC 79211-218 Sanihands

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79211-218?
  4. Sanihands 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:
79211-218
Proprietary Name:
Sanihands
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Porter Aerospace, Llc
Labeler Code:
79211
Product Label ID:
a83b69a8-a45b-c5cf-e053-2a95a90ad69d
Start Marketing Date: [9]
07-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 79211-218?

The NDC code 79211-218 is assigned by the FDA to the product Sanihands which is product labeled by Porter Aerospace, Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 79211-218-18 180 ml in 1 bottle, pump , 79211-218-51 50 ml in 1 bottle, pump , 79211-218-52 500 ml in 1 bottle, plastic , 79211-218-53 5000 ml in 1 bottle, plastic . 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 Sanihands?

- For hand sanitizing to decrease bacteria on the skin. - Recommended for repeated use.

Which are Sanihands UNII Codes?

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

Which are Sanihands 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:

* Please review the disclaimer below.

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".