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  4. NDC Product Code: 43196-510 Opi Antiseptic Foaming Hand Cleaner

NDC 43196-510 Opi Antiseptic Foaming Hand Cleaner

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43196-510?
  4. Opi Antiseptic Foaming Hand Cleaner Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
43196-510
Proprietary Name:
Opi Antiseptic Foaming Hand Cleaner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Opi Correctional Industries
Labeler Code:
43196
Product Label ID:
07177a9e-d1b0-4ce6-9da9-3c24454d715f
Start Marketing Date: [9]
03-07-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43196-510-05

Package Description: 3785 mL in 1 BOTTLE

Product Details

What is NDC 43196-510?

The NDC code 43196-510 is assigned by the FDA to the product Opi Antiseptic Foaming Hand Cleaner which is product labeled by Opi Correctional Industries. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43196-510-05 3785 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 Opi Antiseptic Foaming Hand Cleaner?

Apply cleaner to palm of hand Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 60 seconds Rinse with water until all cleaner is removed from hands Dry completely (incomplete drying may lead to chapped skin).

Which are Opi Antiseptic Foaming Hand Cleaner UNII Codes?

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

Which are Opi Antiseptic Foaming Hand Cleaner 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 Opi Antiseptic Foaming Hand Cleaner?

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".