NDC 10685-511 Pc511 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:
10685-511
Proprietary Name:
Pc511 Antimicrobial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Carroll Company
Labeler Code:
10685
Start Marketing Date: [9]
10-16-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)

Product Packages

NDC Code 10685-511-17

Package Description: 800 mL in 1 BAG

Product Details

What is NDC 10685-511?

The NDC code 10685-511 is assigned by the FDA to the product Pc511 Antimicrobial which is product labeled by Carroll Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10685-511-17 800 ml in 1 bag . 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 Pc511 Antimicrobial?

 apply small amount of product to hands.  hold hands under water and work cleaner into lather.   rinse hands with water and wipe clean.

Which are Pc511 Antimicrobial UNII Codes?

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

Which are Pc511 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 Pc511 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:

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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".