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NDC 80320-001 Its Nanoed Hand

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80320-001?
  4. Its Nanoed Hand 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:
80320-001
Proprietary Name:
Its Nanoed Hand
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
It's Nanoed, Inc.
Labeler Code:
80320
Product Label ID:
b17b1b04-592f-1727-e053-2995a90ad13e
Start Marketing Date: [9]
09-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80320-001-01

Package Description: 3785 mL in 1 BOTTLE

NDC Code 80320-001-02

Package Description: 59 mL in 1 BOTTLE

NDC Code 80320-001-16

Package Description: 473 mL in 1 BOTTLE

NDC Code 80320-001-55

Package Description: 208198 mL in 1 CONTAINER

NDC Code 80320-001-75

Package Description: 1040875 mL in 1 CONTAINER

Product Details

What is NDC 80320-001?

The NDC code 80320-001 is assigned by the FDA to the product Its Nanoed Hand which is product labeled by It's Nanoed, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 80320-001-01 3785 ml in 1 bottle , 80320-001-02 59 ml in 1 bottle , 80320-001-16 473 ml in 1 bottle , 80320-001-55 208198 ml in 1 container , 80320-001-75 1040875 ml in 1 container . 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 Its Nanoed Hand?

On dry hands, place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until hands are entirely dry.

Which are Its Nanoed Hand UNII Codes?

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

Which are Its Nanoed Hand 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".