NDC 75437-001 Slight Acid Hypochlorous Acid Disinfectant

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:
75437-001
Proprietary Name:
Slight Acid Hypochlorous Acid Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
75437
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 75437-001?

The NDC code 75437-001 is assigned by the FDA to the product Slight Acid Hypochlorous Acid Disinfectant which is product labeled by Guangdong Huarui Technology Co., Ltd.. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 75437-001-01 .1 l in 1 bottle , 75437-001-02 .5 l in 1 bottle , 75437-001-03 1 l in 1 bottle , 75437-001-04 5 l in 1 bottle , 75437-001-05 10 l in 1 bottle , 75437-001-06 20 l 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 Slight Acid Hypochlorous Acid Disinfectant?

1. Disinfection of human body. can be used for hand disinfection, spray or rinsed withdisinfectant:2. Disinfection of public space suitable for disinfection of floor and tables and chairsof all materials, spray and wipe directly with the orginal solution of this product.3. Disinfection of air: Spray directly into the air.4. Disinfection of food: Fruits and vegetables disinfection, spray and wipe directlywith this product:5. Disinfection of other appliances: Soak for 5 minutes

Which are Slight Acid Hypochlorous Acid Disinfectant UNII Codes?

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

Which are Slight Acid Hypochlorous Acid Disinfectant 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".