NDC 76772-035 Antibacterial

Product Information

What is NDC 76772-035?

The NDC code 76772-035 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 and is administered via form. The product is distributed in a single package with assigned NDC code 76772-035-33 332 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, RxNorm crosswalk and the complete product label.

NDC Product Code76772-035
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Antibacterial
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Tsm Ithalat Ihracat Sanayi Ve Dis Ticaret Limited Sirketi
Labeler Code76772
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		07-16-2021
Listing Expiration Date 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.		12-31-2022
Exclude Flag 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". 		I
NDC Code Structure

What are the uses for Antibacterial?


Product Packages

NDC Code 76772-035-33

Package Description: 332 mL in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Antibacterial Active Ingredients UNII Codes

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.

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Antibacterial Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredients



Benzalkonium chloride 0.13%.................Anitbacterial Hand soap


Purpose



Antibacterial Hand Soap


Use



helps eliminate bacteria on hands.


Warnings



For external use only: hands only


When Using This Product



  • avoid contact with eyes.  
  • In case of contact,
  • flush with water 

Stop Use And Ask A Doctor If



  • irritation or redness develops
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children



If swallowed, get medical help or contact a Poison Control Center right away


Directions



  • Wet hands and apply soap.
  • Lather front and back, between your fingers and under your nails.
  • Scrub for at least 20 seconds
  • rinse and dry

Inactive Ingredient



Water, Cetrimonium Chloride , Cocamidopropyl Betaine, Sodium Chloride, Glycerin,

Fragrance, Polyquatemium-10 , PEG-8 , Citric Acid, Tetrasodium EDTA, Cocamidopropyl PG-Dimonium Chrolide,

Methylchloroisothiazolinone, Methlisothiazolinone, Blue 1,Red 33


Principal Display Panel



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* Please review the disclaimer below.