NDC 81011-128 Hand 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:
81011-128
Proprietary Name:
Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Design Element Group Inc
Labeler Code:
81011
Start Marketing Date: [9]
11-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Product Packages

NDC Code 81011-128-01

Package Description: 240 mL in 1 BOTTLE

NDC Code 81011-128-02

Package Description: 500 mL in 1 BOTTLE

NDC Code 81011-128-03

Package Description: 1000 mL in 1 BOTTLE

NDC Code 81011-128-04

Package Description: 3785 mL in 1 BOTTLE, PUMP

NDC Code 81011-128-05

Package Description: 1000 mL in 1 POUCH

Product Details

What is NDC 81011-128?

The NDC code 81011-128 is assigned by the FDA to the product Hand Sanitizer which is product labeled by Design Element Group Inc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 81011-128-01 240 ml in 1 bottle , 81011-128-02 500 ml in 1 bottle , 81011-128-03 1000 ml in 1 bottle , 81011-128-04 3785 ml in 1 bottle, pump , 81011-128-05 1000 ml in 1 pouch . 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?

Help decrease bacteria on skin.Pump as needed into your palms & thoroughly spread on both hands.

Which are Hand Sanitizer UNII Codes?

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

Which are Hand 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:

  • WATER (UNII: 059QF0KO0R)
  • FRAGRANCE FRESHWATER CUCUMBER ORC2000871 (UNII: NL1QX9C6TG)
  • ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
  • SULISOBENZONE (UNII: 1W6L629B4K)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

What is the NDC to RxNorm Crosswalk for Hand Sanitizer?

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".