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  4. NDC Product Code: 80431-001 Del Lago Resort And Casino Hand Santitizer

NDC 80431-001 Del Lago Resort And Casino Hand Santitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80431-001?
  4. Del Lago Resort And Casino Hand Santitizer Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
80431-001
Proprietary Name:
Del Lago Resort And Casino Hand Santitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lago Resort & Casino, Llc
Labeler Code:
80431
Product Label ID:
ae5c98db-c5af-8f1f-e053-2995a90a1b58
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80431-001-01

Package Description: 3785 mL in 1 BOTTLE

NDC Code 80431-001-16

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 80431-001?

The NDC code 80431-001 is assigned by the FDA to the product Del Lago Resort And Casino Hand Santitizer which is product labeled by Lago Resort & Casino, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 80431-001-01 3785 ml in 1 bottle , 80431-001-16 500 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 Del Lago Resort And Casino Hand Santitizer?

Wet hands thoroughly with product, and allow to dry without wiping. For children under six, use only under adult supervision.

Which are Del Lago Resort And Casino Hand Santitizer UNII Codes?

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

Which are Del Lago Resort And Casino Hand Santitizer 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".