NDC 80428-109 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:
80428-109
Proprietary Name:
Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rack Furniture Group For Children, Llc.
Labeler Code:
80428
Start Marketing Date: [9]
03-30-2020
End Marketing Date: [10]
03-30-2049
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 80428-109-01

Package Description: 59.2 LIQUID in 1 BOTTLE

Product Details

What is NDC 80428-109?

The NDC code 80428-109 is assigned by the FDA to the product Hand Sanitizer which is product labeled by Rack Furniture Group For Children, Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80428-109-01 59.2 liquid 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?

Briskly rub generous amount on hands and rub together until dry.

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:

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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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".