NDC 78637-101 Gel Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 78637-101?
What are the uses for Gel Hand Sanitizer?
Which are Gel 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 Gel 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:
- LINALYL ACETATE (UNII: 5K47SSQ51G)
- .ALPHA.-METHYLBENZYL ACETATE (UNII: FYS3E9NBA3)
- 2,6,10-TRIMETHYL-9-UNDECENAL (UNII: JNM5JFE28J)
- 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA)
- 2-METHYLUNDECANAL (UNII: S94QNS2VY5)
- WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)
- ORANGE OIL (UNII: AKN3KSD11B)
- 2-ACETONAPHTHONE (UNII: 21D49LOP2T)
- DECANAL (UNII: 31Z90Q7KQJ)
- 2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE (UNII: 452GFV2AFS)
- CYCLAMEN ALDEHYDE (UNII: 4U37UX0E1E)
- 1H,5H-CYCLOPENTA(3,4)(1)BENZOPYRANO(6,7,8-IJ)QUINOLIZIN-12(9H)-ONE, 2,3,6,7,10,11-HEXAHYDRO- (UNII: 9RGV583D48)
- 10-UNDECENAL (UNII: DU1OTA08RY)
- CITRONELLA OIL (UNII: QYO8Q067D0)
- GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S)
- GRAPEFRUIT OIL (UNII: YR377U58W9)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- WATER (UNII: 059QF0KO0R)
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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".