NDC 79175-003 Kellys Delight Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 79175-003?
What are the uses for Kellys Delight Hand Sanitizer?
Which are Kellys Delight 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 Kellys Delight 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- ADENOSINE PHOSPHATE (UNII: 415SHH325A)
- ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- 1-(2,3,8,8-TETRAMETHYL-1,2,3,4,5,6,7,8-OCTAHYDRONAPHTHALEN-2-YL)ETHANONE (UNII: 1GD7ODM28Y)
- LINALYL ACETATE (UNII: 5K47SSQ51G)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
- ETHYL LINALOOL (UNII: SF2JS9GF5T)
- 2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- 3-HEXENYL SALICYLATE, CIS- (UNII: C78Y9OR6YH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
What is the NDC to RxNorm Crosswalk for Kellys Delight Hand Sanitizer?
- 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".