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  4. NDC Product Code: 80155-102 Antibacterial Hand Sanitizer

NDC 80155-102 Antibacterial Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80155-102?
  4. Antibacterial 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:
80155-102
Proprietary Name:
Antibacterial Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Vivian Household Products Co.,ltd
Labeler Code:
80155
Product Label ID:
397761ba-9351-4a64-83bd-05426179d977
Start Marketing Date: [9]
09-23-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 80155-102?

The NDC code 80155-102 is assigned by the FDA to the product Antibacterial Hand Sanitizer which is product labeled by Hangzhou Vivian Household Products Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80155-102-01 250 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 Antibacterial Hand Sanitizer?

Wet your hands with running water, get some hand sanitizer on hands, rub your hands away from each other, and rub the back of your hands, fingers, palms, and nail seams repeatedly in a circular motion.After about 2 minutes, rinse the foam with hands under running water.Wipe hands with a dry clothOther Information:Store below 110℉（43℃）

Which are Antibacterial Hand Sanitizer UNII Codes?

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

Which are Antibacterial 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".