NDC 80224-2000 Nano - Q1

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
80224-2000
Proprietary Name:
Nano - Q1
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Grupo Tma Tecnologias Para El Mejoramiento Del Agua S.a. De C.v.
Labeler Code:
80224
Start Marketing Date: [9]
01-07-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 80224-2000-1

Package Description: 55 mL in 1 BOTTLE, SPRAY

NDC Code 80224-2000-2

Package Description: 120 mL in 1 BOTTLE, SPRAY

NDC Code 80224-2000-3

Package Description: 490 mL in 1 BOTTLE, SPRAY

NDC Code 80224-2000-4

Package Description: 990 mL in 1 BOTTLE, SPRAY

NDC Code 80224-2000-5

Package Description: 5000 mL in 1 JUG

NDC Code 80224-2000-6

Package Description: 10000 mL in 1 JUG

NDC Code 80224-2000-7

Package Description: 20000 mL in 1 JUG

Product Details

What is NDC 80224-2000?

The NDC code 80224-2000 is assigned by the FDA to the product Nano - Q1 which is product labeled by Grupo Tma Tecnologias Para El Mejoramiento Del Agua S.a. De C.v.. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 80224-2000-1 55 ml in 1 bottle, spray , 80224-2000-2 120 ml in 1 bottle, spray , 80224-2000-3 490 ml in 1 bottle, spray , 80224-2000-4 990 ml in 1 bottle, spray , 80224-2000-5 5000 ml in 1 jug , 80224-2000-6 10000 ml in 1 jug , 80224-2000-7 20000 ml in 1 jug . 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 Nano - Q1?

This product is used as Purpose: Antimicrobial, Bactericide, Virucidal. Use[s]Skin, objects and surface sanitizer to help reduce bacteria and viruses

Which are Nano - Q1 UNII Codes?

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

Which are Nano - Q1 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".