1. Home
  2. Labeler Index
  3. Best Sanitizers, Inc
  4. NDC Product Code: 59900-114 Smart San Es Hand Sanitizer Spray

NDC 59900-114 Smart San Es Hand Sanitizer Spray

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59900-114?
  4. Smart San Es Hand Sanitizer Spray Uses
  5. Active Ingredients UNII Codes
  6. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59900-114
Proprietary Name:
Smart San Es Hand Sanitizer Spray
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Best Sanitizers, Inc
Labeler Code:
59900
Product Label ID:
be2b86fb-a950-4941-aa68-a9bd7df1d759
Start Marketing Date: [9]
07-01-2004
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 59900-114?

The NDC code 59900-114 is assigned by the FDA to the product Smart San Es Hand Sanitizer Spray which is product labeled by Best Sanitizers, Inc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 59900-114-02 3785 ml in 1 bottle, plastic , 59900-114-03 189250 ml in 1 drum , 59900-114-04 500 ml in 1 bottle, plastic , 59900-114-05 1000 ml in 1 bottle, plastic , 59900-114-06 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 Smart San Es Hand Sanitizer Spray?

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

Which are Smart San Es Hand Sanitizer Spray UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Smart San Es 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:

* Please review the disclaimer below.

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".