1. Home
  2. Labeler Index
  3. Beauty-lab Llc
  4. NDC Product Code: 80473-030 Clean Is In Hand Sanitizer Antiseptic Foam

NDC 80473-030 Clean Is In Hand Sanitizer Antiseptic Foam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80473-030?
  4. Clean Is In Hand Sanitizer Antiseptic Foam Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
80473-030
Proprietary Name:
Clean Is In Hand Sanitizer Antiseptic Foam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Beauty-lab Llc
Labeler Code:
80473
Product Label ID:
21b74828-9b7b-42c9-b4ea-034e7ee94ddf
Start Marketing Date: [9]
09-10-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 80473-030?

The NDC code 80473-030 is assigned by the FDA to the product Clean Is In Hand Sanitizer Antiseptic Foam which is product labeled by Beauty-lab Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80473-030-01 200 g in 1 container . 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 Clean Is In Hand Sanitizer Antiseptic Foam?

This product is used as Active Ingredient.....................PurposeAlcohol 62% v/v........................................Antiseptic. Uses•To help decrease bacteria/germs on the skin.•For usewhen soap and water are not available.•Recommended forrepeated use.

Which are Clean Is In Hand Sanitizer Antiseptic Foam UNII Codes?

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

Which are Clean Is In Hand Sanitizer Antiseptic Foam 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:

What is the NDC to RxNorm Crosswalk for Clean Is In Hand Sanitizer Antiseptic Foam?

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".