NDC 21749-480 Purell Advanced Skin Balancing 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:
21749-480
Proprietary Name:
Purell Advanced Skin Balancing Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
21749
Start Marketing Date: [9]
12-30-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 21749-480?

The NDC code 21749-480 is assigned by the FDA to the product Purell Advanced Skin Balancing Hand Sanitizer which is product labeled by Gojo Industries, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 21749-480-01 30 ml in 1 bottle , 21749-480-02 59 ml in 1 bottle , 21749-480-08 236 ml in 1 bottle , 21749-480-12 354 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 Purell Advanced Skin Balancing Hand Sanitizer?

Place enough product in your palm to thoroughly cover your handsRub hands together briskly until dryChildren under 6 years of age should be supervised when using this product.

Which are Purell Advanced Skin Balancing Hand Sanitizer UNII Codes?

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

Which are Purell Advanced Skin Balancing 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:

What is the NDC to RxNorm Crosswalk for Purell Advanced Skin Balancing 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".