NDC 79741-003 Kleen Hand Sanitizer Mango
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 79741-003?
What are the uses for Kleen Hand Sanitizer Mango?
Which are Kleen Hand Sanitizer Mango UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Kleen Hand Sanitizer Mango 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:
- DIETHYL MALONATE (UNII: 53A58PA183)
- BORNYL ACETATE, (-)- (UNII: 24QAP1VCUX)
- HEXYL ACETATE (UNII: 7U7KU3MWT0)
- 2-TERT-BUTYLCYCLOHEXYL ACETATE (UNII: 364FV60913)
- ETHYL LINALOOL (UNII: SF2JS9GF5T)
- ETHYL MALTOL (UNII: L6Q8K29L05)
- HEXAHYDRO-4,7-METHANOINDEN-6-YL PROPIONATE (UNII: S3ASM14UAS)
- 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- 2-(2-(4-METHYLCYCLOHEX-3-EN-1-YL)PROPYL)CYCLOPENTAN-1-ONE (UNII: P1K3Z8A8HJ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- HEXYL SALICYLATE (UNII: 8F78EY72YL)
- 1-(2,3,8,8-TETRAMETHYL-1,2,3,4,5,6,7,8-OCTAHYDRONAPHTHALEN-2-YL)ETHANONE (UNII: 1GD7ODM28Y)
- TROLAMINE (UNII: 9O3K93S3TK)
- .GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL)
- WATER (UNII: 059QF0KO0R)
- 3-HEXENYL SALICYLATE, CIS- (UNII: C78Y9OR6YH)
What is the NDC to RxNorm Crosswalk for Kleen Hand Sanitizer Mango?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
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[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".