NDC 50563-195 Clean Hands Antibacterial Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50563 - Enchante Accessories Inc.
- 50563-195 - Clean Hands Antibacterial Hand Sanitizer
Product Packages
NDC Code 50563-195-01
Package Description: 200 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
NDC Code 50563-195-02
Package Description: 150 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE
NDC Code 50563-195-03
Package Description: 100 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE
NDC Code 50563-195-04
Package Description: 24 BOTTLE in 1 CARTON / 237 mL in 1 BOTTLE
NDC Code 50563-195-05
Package Description: 20 BOTTLE in 1 CARTON / 500 mL in 1 BOTTLE
NDC Code 50563-195-06
Package Description: 18 BOTTLE in 1 CARTON / 1000 mL in 1 BOTTLE
NDC Code 50563-195-07
Package Description: 4 BOTTLE in 1 CARTON / 3780 mL in 1 BOTTLE
NDC Code 50563-195-08
Package Description: 4 BOTTLE in 1 CARTON / 5000 mL in 1 BOTTLE
Product Details
What is NDC 50563-195?
What are the uses for Clean Hands Antibacterial Hand Sanitizer?
Which are Clean Hands Antibacterial Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Clean Hands Antibacterial Hand 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER 934 (UNII: Z135WT9208)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Clean Hands Antibacterial Hand Sanitizer?
- RxCUI: 1305100 - ethanol 75 % Topical Gel
- RxCUI: 1305100 - ethanol 0.75 ML/ML Topical Gel
* 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".