NDC 69139-106 Coralite Antibacterial Bandages
Benzalkonium Chloride Swab Topical
NDC Code 69139-106-01
Package Description: 30 POUCH in 1 BOX / .5 g in 1 POUCH
What is NDC 69139-106?
The NDC code 69139-106 is assigned by the FDA to the product Coralite Antibacterial Bandages which is a human over the counter drug product labeled by Yiwu Haoding Medical Co.,ltd. The generic name of Coralite Antibacterial Bandages is benzalkonium chloride. The product's dosage form is swab and is administered via topical form. The product is distributed in a single package with assigned NDC code 69139-106-01 30 pouch in 1 box / .5 g in 1 pouch. 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 Coralite Antibacterial Bandages?
This product is used as Antiseptic
What are Coralite Antibacterial Bandages Active Ingredients?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
Which are Coralite Antibacterial Bandages UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Coralite Antibacterial Bandages 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:
- WATER (UNII: 059QF0KO0R)
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