NDC 41190-210 Advanced Antiseptic

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:
41190-210
Proprietary Name:
Advanced Antiseptic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wakefern Food Corporation
Labeler Code:
41190
Start Marketing Date: [9]
11-24-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41190-210-12

Package Description: 1.5 L in 1 BOTTLE, PLASTIC

NDC Code 41190-210-86

Package Description: 1 L in 1 BOTTLE, PLASTIC

Product Details

What is NDC 41190-210?

The NDC code 41190-210 is assigned by the FDA to the product Advanced Antiseptic which is product labeled by Wakefern Food Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 41190-210-12 1.5 l in 1 bottle, plastic , 41190-210-86 1 l 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 Advanced Antiseptic?

Use helps control plaque that leads to gingivitis

Which are Advanced Antiseptic UNII Codes?

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

Which are Advanced Antiseptic 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:

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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".