NDC 33992-3028 Hand Sanitizer Refill 15 Oz

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:
33992-3028
Proprietary Name:
Hand Sanitizer Refill 15 Oz
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Greenbrier International, Inc.
Labeler Code:
33992
Start Marketing Date: [9]
01-02-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Score:
1

Product Packages

NDC Code 33992-3028-1

Package Description: 443 mL in 1 BOTTLE

Product Details

What is NDC 33992-3028?

The NDC code 33992-3028 is assigned by the FDA to the product Hand Sanitizer Refill 15 Oz which is product labeled by Greenbrier International, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 33992-3028-1 443 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 Hand Sanitizer Refill 15 Oz?

For handwashing to decrease bacteria on the skin recommended for repeated use

Which are Hand Sanitizer Refill 15 Oz UNII Codes?

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

Which are Hand Sanitizer Refill 15 Oz 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 Hand Sanitizer Refill 15 Oz?

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:

* Please review the disclaimer below.

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".