NDC 60193-200 Woodwards Handclens Foaming Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60193 - Pacific World Corporation
- 60193-200 - Woodwards Handclens Foaming Sanitizer
Product Packages
NDC Code 60193-200-01
Package Description: 236 mL in 1 BOTTLE, PUMP
NDC Code 60193-200-03
Package Description: 1000 mL in 1 CARTRIDGE
NDC Code 60193-200-05
Package Description: 1800 mL in 1 BOTTLE, PUMP
NDC Code 60193-200-07
Package Description: 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 60193-200?
What are the uses for Woodwards Handclens Foaming Sanitizer?
Which are Woodwards Handclens Foaming Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Woodwards Handclens Foaming Sanitizer 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)
- DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- ALLANTOIN (UNII: 344S277G0Z)
- COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALCOHOL (UNII: 3K9958V90M)
What is the NDC to RxNorm Crosswalk for Woodwards Handclens Foaming Sanitizer?
- RxCUI: 1020365 - benzalkonium chloride 0.13 % Topical Foam
- RxCUI: 1020365 - benzalkonium chloride 1.3 MG/ML Topical Foam
- RxCUI: 1426841 - HandClens 0.13 % Topical Foam
- RxCUI: 1426841 - benzalkonium chloride 1.3 MG/ML Topical Foam [Handclens]
- RxCUI: 1426841 - Handclens 0.13 % Topical Foam
* 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".