NDC 62742-4184 Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs Inc
- 62742-4184 - Hand Sanitizer
Product Packages
NDC Code 62742-4184-1
Package Description: 59.14 mL in 1 BOTTLE, PUMP
NDC Code 62742-4184-2
Package Description: 355 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 62742-4184?
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)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- TROLAMINE (UNII: 9O3K93S3TK)
- BENZYL BENZOATE (UNII: N863NB338G)
- CITRAL (UNII: T7EU0O9VPP)
- GERANIOL (UNII: L837108USY)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % 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".