NDC 73357-627 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 73357-627-00
Package Description: 100 mL in 1 BOTTLE
NDC Code 73357-627-01
Package Description: 20 mL in 1 BOTTLE
NDC Code 73357-627-02
Package Description: 200 mL in 1 BOTTLE
NDC Code 73357-627-03
Package Description: 300 mL in 1 BOTTLE
NDC Code 73357-627-05
Package Description: 50 mL in 1 BOTTLE
NDC Code 73357-627-08
Package Description: 8 mL in 1 BOTTLE
NDC Code 73357-627-09
Package Description: 90 mL in 1 BOTTLE
NDC Code 73357-627-10
Package Description: 10 mL in 1 BOTTLE
NDC Code 73357-627-15
Package Description: 15 mL in 1 BOTTLE
NDC Code 73357-627-20
Package Description: 120 mL in 1 BOTTLE
NDC Code 73357-627-24
Package Description: 240 mL in 1 BOTTLE
NDC Code 73357-627-25
Package Description: 250 mL in 1 BOTTLE
NDC Code 73357-627-29
Package Description: 29 mL in 1 BOTTLE
NDC Code 73357-627-30
Package Description: 30 mL in 1 BOTTLE
NDC Code 73357-627-35
Package Description: 350 mL in 1 BOTTLE
NDC Code 73357-627-50
Package Description: 150 mL in 1 BOTTLE
NDC Code 73357-627-51
Package Description: 500 mL in 1 BOTTLE
NDC Code 73357-627-55
Package Description: 5 mL in 1 BOTTLE
NDC Code 73357-627-60
Package Description: 60 mL in 1 BOTTLE
NDC Code 73357-627-80
Package Description: 80 mL in 1 BOTTLE
Product Details
What is NDC 73357-627?
What are the uses for Hand Sanitizer?
Which are 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 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)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 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".