1. Home
  2. Labeler Index
  3. Carroll Company
  4. NDC Product Code: 10685-537 Pc537 E-2 Brute

NDC 10685-537 Pc537 E-2 Brute

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10685-537?
  5. Pc537 E-2 Brute Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
10685-537
Proprietary Name:
Pc537 E-2 Brute
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Carroll Company
Labeler Code:
10685
Product Label ID:
1255b618-5528-4443-8ba3-71d2eb95f5f7
Start Marketing Date: [9]
10-16-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 10685-537?

The NDC code 10685-537 is assigned by the FDA to the product Pc537 E-2 Brute which is product labeled by Carroll Company. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10685-537-11 208000 ml in 1 drum , 10685-537-28 3785 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 Pc537 E-2 Brute?

 wet hands  apply liberal quantity to hands  contact time of one minute is recommended  rinse hands thoroughly with potable water.

Which are Pc537 E-2 Brute UNII Codes?

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

Which are Pc537 E-2 Brute 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 Pc537 E-2 Brute?

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".