NDC 74052-337 Iris Hand Sanitizer Gel

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:
74052-337
Proprietary Name:
Iris Hand Sanitizer Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Iris Llc
Labeler Code:
74052
Start Marketing Date: [9]
04-03-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 74052-337-01

Package Description: 30 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-02

Package Description: 59 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-03

Package Description: 100 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-04

Package Description: 118 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-08

Package Description: 237 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-10

Package Description: 296 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-12

Package Description: 355 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-16

Package Description: 473 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-17

Package Description: 500 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-28

Package Description: 3785.41 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-34

Package Description: 1000 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-38

Package Description: 18927.1 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-55

Package Description: 208198 mL in 1 BOTTLE, PUMP

NDC Code 74052-337-99

Package Description: 1041000 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 74052-337?

The NDC code 74052-337 is assigned by the FDA to the product Iris Hand Sanitizer Gel which is product labeled by Iris Llc. The product's dosage form is . The product is distributed in 14 packages with assigned NDC codes 74052-337-01 30 ml in 1 bottle, pump , 74052-337-02 59 ml in 1 bottle, pump , 74052-337-03 100 ml in 1 bottle, pump , 74052-337-04 118 ml in 1 bottle, pump , 74052-337-08 237 ml in 1 bottle, pump , 74052-337-10 296 ml in 1 bottle, pump , 74052-337-12 355 ml in 1 bottle, pump , 74052-337-16 473 ml in 1 bottle, pump , 74052-337-17 500 ml in 1 bottle, pump , 74052-337-28 3785.41 ml in 1 bottle, pump , 74052-337-34 1000 ml in 1 bottle, pump , 74052-337-38 18927.1 ml in 1 bottle, pump , 74052-337-55 208198 ml in 1 bottle, pump , 74052-337-99 1041000 ml in 1 bottle, pump . 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 Iris Hand Sanitizer Gel?

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Which are Iris Hand Sanitizer Gel UNII Codes?

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

Which are Iris Hand Sanitizer Gel 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:

What is the NDC to RxNorm Crosswalk for Iris Hand Sanitizer Gel?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".