NDC 69540-0029 Clorox Antimicrobial

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:
69540-0029
Proprietary Name:
Clorox Antimicrobial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Brand Buzz Llc
Labeler Code:
69540
Start Marketing Date: [9]
04-07-2014
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
MENTHOL (C73403)

Product Packages

NDC Code 69540-0029-1

Package Description: 650 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 69540-0029?

The NDC code 69540-0029 is assigned by the FDA to the product Clorox Antimicrobial which is product labeled by Brand Buzz Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69540-0029-1 650 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 Clorox Antimicrobial?

Apply onto wet hands, lather for 30 seconds and rinse thoroughly.

Which are Clorox Antimicrobial UNII Codes?

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

Which are Clorox Antimicrobial 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 Clorox Antimicrobial?

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:
  • RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap

* 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".