NDC 62257-014 1014 Foaming Antimicrobial
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 62257-014-01
Package Description: 1200 mL in 1 CARTRIDGE
NDC Code 62257-014-03
Package Description: 350 mL in 1 CARTRIDGE
NDC Code 62257-014-05
Package Description: 540 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-06
Package Description: 1 BAG in 1 BOX / 800 mL in 1 BAG
NDC Code 62257-014-07
Package Description: 700 mL in 1 BAG
NDC Code 62257-014-08
Package Description: 1 BAG in 1 BOX / 1000 mL in 1 BAG
NDC Code 62257-014-09
Package Description: 2000 mL in 1 CARTRIDGE
NDC Code 62257-014-10
Package Description: 1000 mL in 1 CARTRIDGE
NDC Code 62257-014-11
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-12
Package Description: 1000 mL in 1 BAG
NDC Code 62257-014-13
Package Description: 800 mL in 1 BAG
NDC Code 62257-014-14
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-15
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-16
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-17
Package Description: 532 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-18
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-24
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-27
Package Description: 800 mL in 1 CARTRIDGE
NDC Code 62257-014-28
Package Description: 149 mL in 1 BOTTLE, PLASTIC
NDC Code 62257-014-55
Package Description: 208200 mL in 1 DRUM
Product Details
What is NDC 62257-014?
What are the uses for 1014 Foaming Antimicrobial?
Which are 1014 Foaming Antimicrobial UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are 1014 Foaming Antimicrobial 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- BORIC ACID (UNII: R57ZHV85D4)
- ALCOHOL (UNII: 3K9958V90M)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- EDETATE SODIUM (UNII: MP1J8420LU)
* Please review the disclaimer below.
[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".