NDC 65601-741 Triton Ab-741

NDC Product Code 65601-741

NDC CODE: 65601-741

Proprietary Name: Triton Ab-741 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.

NDC Code Structure

  • 65601 - Betco Corporation, Ltd.

NDC 65601-741-62

Package Description: 2000 mL in 1 BOTTLE, DISPENSING

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

NDC Product Information

Triton Ab-741 with NDC 65601-741 is a product labeled by Betco Corporation, Ltd.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1362618.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Betco Corporation, Ltd.
Labeler Code: 65601
Start Marketing Date: 11-12-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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Triton Ab-741 Product Label Images

Triton Ab-741 Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Triton Ab-741

​Active IngredientChloroxylenol 0.375%

  • Uses​​Antibacterial hand cleaner.Use in daycare, hospitals, nursing homes, physicians offices, dental offices and clinics

  • WarningsFor external use only.Avoid contact with eyes.Children under the age of 6 should be supervised by an adult when using this product.Discontinue use is irritation or redness develops.If irritation persists for more than 72 hours, consult a physician.KEEP OUT OF REACH OF CHILDREN.

  • Directions​Read the entire label before using this product.​Dispense 1-2 pumps of product onto wet palm.Lather and rinse hands with clean water

Inactive Ingredients​Water, Sodium Lauryl lSulfate, Cocamide DEA, Cocamidopropyl betadine, Phenoxyethanol, Sodium Laureth Sulfate, Propylene Glycol, Fragrance, DMDM Hydantoin, Glycol Stearate, Laurimide DEA, Glycerine, Tocopheryl Acetate, D&C Green #5, FD&C Yellow #5.

Questions or Comments?Phone: (800) 777-9343MDS information:​(800) 891-4965


Winning Hands AntibacterialKEEP OUT OF REACH OF CHILDREN

Triton AB-741Antibacterial Skin CleanserAntibacterial Lotion Skin Cleanser with Chloroxylenol (PCMX)Net Contents: 2 LItem #: 74162-00MSDS No.:7412007 Betco CorprorationToledo Ohio 43607-0127 Made in the U.S.A.All Rights Reserved. www.betco.com

* Please review the disclaimer below.