NDC 79392-102 Antiseptic Liquid

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:
79392-102
Proprietary Name:
Antiseptic Liquid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
79392
Start Marketing Date: [9]
07-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 79392-102?

The NDC code 79392-102 is assigned by the FDA to the product Antiseptic Liquid which is product labeled by Itimat Kozmetik Urunleri Sanayi Ve Ticaret Anonim Sirketi. The product's dosage form is . The product is distributed in 18 packages with assigned NDC codes 79392-102-01 50 ml in 1 bottle , 79392-102-02 100 ml in 1 bottle , 79392-102-03 150 ml in 1 bottle , 79392-102-04 250 ml in 1 bottle , 79392-102-05 500 ml in 1 bottle , 79392-102-06 750 ml in 1 bottle , 79392-102-07 1000 ml in 1 bottle , 79392-102-08 1500 ml in 1 bottle , 79392-102-09 2000 ml in 1 bottle , 79392-102-10 2500 ml in 1 bottle , 79392-102-11 3000 ml in 1 bottle , 79392-102-12 3500 ml in 1 bottle , 79392-102-13 4000 ml in 1 bottle , 79392-102-14 4500 ml in 1 bottle , 79392-102-15 5000 ml in 1 bottle , 79392-102-16 10000 ml in 1 bottle , 79392-102-17 20000 ml in 1 bottle , 79392-102-18 36 bottle in 1 box / 50 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 Antiseptic Liquid?

• Squeeze a few pumps into your palms, foam with water and rinse.• supervise children under 6 years of age when using this product to avoid swallowing

Which are Antiseptic Liquid UNII Codes?

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

Which are Antiseptic Liquid 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 Antiseptic Liquid?

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".