NDC 59900-107 Alpet E3 Hand Sanitizer Spray

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:
59900-107
Proprietary Name:
Alpet E3 Hand Sanitizer Spray
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Best Sanitizer, Inc.
Labeler Code:
59900
Start Marketing Date: [9]
01-01-1995
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59900-107-02

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Code 59900-107-03

Package Description: 208175 mL in 1 DRUM

NDC Code 59900-107-04

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 59900-107-05

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 59900-107-06

Package Description: 59 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 59900-107?

The NDC code 59900-107 is assigned by the FDA to the product Alpet E3 Hand Sanitizer Spray which is product labeled by Best Sanitizer, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 59900-107-02 3785 ml in 1 bottle, plastic , 59900-107-03 208175 ml in 1 drum , 59900-107-04 500 ml in 1 bottle, plastic , 59900-107-05 1000 ml in 1 bottle, plastic , 59900-107-06 59 ml in 1 bottle, plastic . 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 Alpet E3 Hand Sanitizer Spray?

Wet hands thoroughly with spray, covering entire surface of hands, especially the fingernails and cuticlesRub hands together until dry

Which are Alpet E3 Hand Sanitizer Spray UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Alpet E3 Hand Sanitizer Spray?

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".