NDC 79175-010 Kellys Delight Hand Sanitizer (apple Cider)
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What is NDC 79175-010?
What are the uses for Kellys Delight Hand Sanitizer (apple Cider)?
Which are Kellys Delight Hand Sanitizer (apple Cider) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Kellys Delight Hand Sanitizer (apple Cider) 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 2-TERT-BUTYLCYCLOHEXYL ACETATE (UNII: 364FV60913)
- METHYL CINNAMATE (UNII: 533CV2ZCQL)
- ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- CARYOPHYLLENE (UNII: BHW853AU9H)
- METHYL DIHYDROJASMONATE, (-)-TRANS- (UNII: XM1C2C5MMN)
- .ALPHA.-ISOPROPYL-PHENETHYL ALCOHOL (UNII: N06AQ6J88Y)
- DIETHYL MALONATE (UNII: 53A58PA183)
What is the NDC to RxNorm Crosswalk for Kellys Delight Hand Sanitizer (apple Cider)?
- 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".