1. Home
  2. Labeler Index
  3. Liquid Labs Llc
  4. NDC Product Code: 77568-123 Keep It Kleen

NDC 77568-123 Keep It Kleen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 77568-123?
  5. Keep It Kleen Uses
  6. Active Ingredients UNII Codes
  7. 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:
77568-123
Proprietary Name:
Keep It Kleen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Liquid Labs Llc
Labeler Code:
77568
Product Label ID:
d4257536-598f-2318-e053-2a95a90a9642
Start Marketing Date: [9]
02-03-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Size(s):
120000 MM

Code Structure Chart

Product Details

What is NDC 77568-123?

The NDC code 77568-123 is assigned by the FDA to the product Keep It Kleen which is product labeled by Liquid Labs Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77568-123-45 1 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 Keep It Kleen?

HAND SANITIZER TO HELP REDUCE BACTERIA THAT POTENTIALLY CAN CAUSE DISEASE. FOR USE WHEN SOAP AND WATER ARE NOT AVAILABLE. FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM HEAT OR FLAM. DO NOT USE IN CHILDREN LESS THAN 2 MONTHS OF AGE OR ON OPEN SKIN WOUNDS

Which are Keep It Kleen UNII Codes?

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

Which are Keep It Kleen 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:

* 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".