NDC 53950-1001 Beclean Hand Sanitizer 75 Percent Alcohol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53950 - World Amenities
- 53950-1001 - Beclean Hand Sanitizer
Product Packages
NDC Code 53950-1001-0
Package Description: 30 mL in 1 BOTTLE
NDC Code 53950-1001-1
Package Description: 1000 mL in 1 BOTTLE
NDC Code 53950-1001-2
Package Description: 500 mL in 1 BOTTLE
NDC Code 53950-1001-3
Package Description: 250 mL in 1 BOTTLE
NDC Code 53950-1001-4
Package Description: 60 mL in 1 BOTTLE
NDC Code 53950-1001-5
Package Description: 3800 mL in 1 BOTTLE
NDC Code 53950-1001-6
Package Description: 2000 mL in 1 BOTTLE
NDC Code 53950-1001-7
Package Description: 3000 mL in 1 BOTTLE
NDC Code 53950-1001-8
Package Description: 5000 mL in 1 BOTTLE
NDC Code 53950-1001-9
Package Description: 30 mL in 1 TUBE
Product Details
What is NDC 53950-1001?
What are the uses for Beclean Hand Sanitizer 75 Percent Alcohol?
Which are Beclean Hand Sanitizer 75 Percent Alcohol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Beclean Hand Sanitizer 75 Percent Alcohol 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)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Beclean Hand Sanitizer 75 Percent Alcohol?
- 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".