NDC 76772-003 Antibacterial

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:
76772-003
Proprietary Name:
Antibacterial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi
Labeler Code:
76772
Start Marketing Date: [9]
05-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 76772-003-80

Package Description: 500 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 76772-003?

The NDC code 76772-003 is assigned by the FDA to the product Antibacterial which is product labeled by Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76772-003-80 500 ml in 1 bottle, pump . 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 Antibacterial?

Wet handsapply palmful to handsscrub thoroughlyrinse toroughly

Which are Antibacterial UNII Codes?

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

Which are Antibacterial 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".