NDC 75862-022 Teacher Collection Anti Bacterial Delicious Apple
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75862 - Ganz U.s.a., Llc
- 75862-022 - Teacher Collection Anti Bacterial
Product Packages
NDC Code 75862-022-01
Package Description: 200 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 75862-022?
What are the uses for Teacher Collection Anti Bacterial Delicious Apple?
Which are Teacher Collection Anti Bacterial Delicious Apple UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Teacher Collection Anti Bacterial Delicious Apple 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
- COW MILK FAT (UNII: 463JZS0XJ3)
- MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)
- SHEA BUTTER (UNII: K49155WL9Y)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- PETROLATUM (UNII: 4T6H12BN9U)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBIC ACID (UNII: X045WJ989B)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
What is the NDC to RxNorm Crosswalk for Teacher Collection Anti Bacterial Delicious Apple?
- RxCUI: 1102185 - benzalkonium chloride 0.1 % Topical Lotion
- RxCUI: 1102185 - benzalkonium chloride 1 MG/ML Topical Lotion
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[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".