NDC 61139-422 Highmark Professional Pink Antimicrobial Ltn Sp

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:
61139-422
Proprietary Name:
Highmark Professional Pink Antimicrobial Ltn Sp
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Office Max, Inc.
Labeler Code:
61139
Start Marketing Date: [9]
11-22-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61139-422-10

Package Description: 1000 mL in 1 BOTTLE

NDC Code 61139-422-20

Package Description: 2000 mL in 1 BOTTLE

NDC Code 61139-422-37

Package Description: 3785 mL in 1 JUG

NDC Code 61139-422-80

Package Description: 800 mL in 1 BAG

NDC Code 61139-422-89

Package Description: 1200 mL in 1 BOTTLE

NDC Code 61139-422-90

Package Description: 1250 mL in 1 BOTTLE

Product Details

What is NDC 61139-422?

The NDC code 61139-422 is assigned by the FDA to the product Highmark Professional Pink Antimicrobial Ltn Sp which is product labeled by Office Max, Inc.. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 61139-422-10 1000 ml in 1 bottle , 61139-422-20 2000 ml in 1 bottle , 61139-422-37 3785 ml in 1 jug , 61139-422-80 800 ml in 1 bag , 61139-422-89 1200 ml in 1 bottle , 61139-422-90 1250 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 Highmark Professional Pink Antimicrobial Ltn Sp?

Wet handsApply a small amount of product and work into a latherRinse well and dry hands completely

Which are Highmark Professional Pink Antimicrobial Ltn Sp UNII Codes?

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

Which are Highmark Professional Pink Antimicrobial Ltn Sp 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".