NDC 76701-362 Hy-iq Hand And Surface Disinfectant And Sanitizer

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:
76701-362
Proprietary Name:
Hy-iq Hand And Surface Disinfectant And Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hand Sanitizer Llc
Labeler Code:
76701
Start Marketing Date: [9]
06-17-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76701-362-02

Package Description: 50.275 mL in 1 BOTTLE, SPRAY

NDC Code 76701-362-16

Package Description: 473.176 mL in 1 BOTTLE, SPRAY

NDC Code 76701-362-32

Package Description: 946.353 mL in 1 BOTTLE, SPRAY

NDC Code 76701-362-76

Package Description: 3785.41 mL in 1 BOTTLE

Product Details

What is NDC 76701-362?

The NDC code 76701-362 is assigned by the FDA to the product Hy-iq Hand And Surface Disinfectant And Sanitizer which is product labeled by Hand Sanitizer Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 76701-362-02 50.275 ml in 1 bottle, spray , 76701-362-16 473.176 ml in 1 bottle, spray , 76701-362-32 946.353 ml in 1 bottle, spray , 76701-362-76 3785.41 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 Hy-iq Hand And Surface Disinfectant And Sanitizer?

For spraying on hands or hard surfaces in order to prevent the spreading of bacteria & harmful germs.

Which are Hy-iq Hand And Surface Disinfectant And Sanitizer UNII Codes?

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

Which are Hy-iq Hand And Surface Disinfectant And 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".