NDC 59555-902 Industrial Sanitizing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59555 - R&r Lotion, Inc.
- 59555-902 - Industrial Sanitizing
Product Characteristics
Product Packages
NDC Code 59555-902-04
Package Description: 59 mL in 1 BOTTLE, PLASTIC
NDC Code 59555-902-07
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC Code 59555-902-08
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Code 59555-902-10
Package Description: 946 mL in 1 BOTTLE, PUMP
NDC Code 59555-902-11
Package Description: 3785 mL in 1 BOTTLE, PUMP
NDC Code 59555-902-13
Package Description: 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 59555-902?
What are the uses for Industrial Sanitizing?
Which are Industrial Sanitizing UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Industrial Sanitizing 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)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- VITAMIN A (UNII: 81G40H8B0T)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
What is the NDC to RxNorm Crosswalk for Industrial Sanitizing?
- RxCUI: 1549533 - benzethonium chloride 0.2 % / dimethicone 2 % Topical Lotion
- RxCUI: 1549533 - benzethonium chloride 2 MG/ML / dimethicone 20 MG/ML Topical Lotion
* 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".