NDC 55863-700 Alcoscrub Hand Cleaner

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:
55863-700
Proprietary Name:
Alcoscrub Hand Cleaner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Erie Scientific, Llc.
Labeler Code:
55863
Start Marketing Date: [9]
01-03-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 55863-700-04

Package Description: 118 mL in 1 BOTTLE

NDC Code 55863-700-16

Package Description: 472 mL in 1 BOTTLE

NDC Code 55863-700-27

Package Description: 800 mL in 1 POUCH

NDC Code 55863-700-32

Package Description: 944 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 55863-700?

The NDC code 55863-700 is assigned by the FDA to the product Alcoscrub Hand Cleaner which is product labeled by Erie Scientific, Llc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 55863-700-04 118 ml in 1 bottle , 55863-700-16 472 ml in 1 bottle , 55863-700-27 800 ml in 1 pouch , 55863-700-32 944 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 Alcoscrub Hand Cleaner?

For hand cleaning to decrease bacteria on skin

Which are Alcoscrub Hand Cleaner UNII Codes?

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

Which are Alcoscrub Hand Cleaner 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.

[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".