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  4. NDC Product Code: 78218-007 Ohtrust Nano Ion Water

NDC 78218-007 Ohtrust Nano Ion Water

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78218-007?
  4. Ohtrust Nano Ion Water 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:
78218-007
Proprietary Name:
Ohtrust Nano Ion Water
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kunshan Nano Environmental Protection Technology Co. Ltd.
Labeler Code:
78218
Product Label ID:
b676c789-121a-68a4-e053-2995a90a16d8
Start Marketing Date: [9]
12-14-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 78218-007?

The NDC code 78218-007 is assigned by the FDA to the product Ohtrust Nano Ion Water which is product labeled by Kunshan Nano Environmental Protection Technology Co. Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78218-007-01 60000 mg 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 Ohtrust Nano Ion Water?

Spray on hands, skin, or places that need to reduce bacteria. After spray, let it dry and no need to rinse.

Which are Ohtrust Nano Ion Water UNII Codes?

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

Which are Ohtrust Nano Ion Water 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".