NDC 76701-361 Hy-iq Surface Cleaner

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:
76701-361
Proprietary Name:
Hy-iq Surface Cleaner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hand Sanitizer Llc
Labeler Code:
76701
Start Marketing Date: [9]
06-21-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76701-361-26

Package Description: 473.176 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 76701-361?

The NDC code 76701-361 is assigned by the FDA to the product Hy-iq Surface Cleaner which is product labeled by Hand Sanitizer Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76701-361-26 473.176 ml 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 Hy-iq Surface Cleaner?

For hand sanitizing. Helps prevent the risk and spread of infection and communicable diseases by killing germs that reside on skin and surfaces.

Which are Hy-iq Surface Cleaner UNII Codes?

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

Which are Hy-iq Surface Cleaner 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".