NDC 42587-001 Frais Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42587 - Frais Luxury Products
- 42587-001 - Frais Hand Sanitizer
Product Packages
NDC Code 42587-001-01
Package Description: 6 g in 1 BOTTLE, PLASTIC
NDC Code 42587-001-02
Package Description: 50 g in 1 BOTTLE, PLASTIC
NDC Code 42587-001-03
Package Description: 444 g in 1 BOTTLE, PUMP
NDC Code 42587-001-04
Package Description: 14 BOTTLE, PLASTIC in 1 BOX / 6 g in 1 BOTTLE, PLASTIC (42587-001-01)
NDC Code 42587-001-05
Package Description: 1 g in 1 PACKET
Product Details
What is NDC 42587-001?
What are the uses for Frais Hand Sanitizer?
Which are Frais 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 Frais 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:
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- WATER (UNII: 059QF0KO0R)
- VACCINIUM MYRTILLUS LEAF (UNII: Y4U591OU70)
- ORANGE (UNII: 5EVU04N5QU)
- GRAPEFRUIT (UNII: O82C39RR8C)
- TANGERINE (UNII: KH3E3096OO)
- CARDAMOM (UNII: 8BC4CUT4JL)
- MELALEUCA QUINQUENERVIA POLLEN (UNII: NX974IRT8E)
- BASIL (UNII: 2U0KZP0FDW)
- GINGER (UNII: C5529G5JPQ)
What is the NDC to RxNorm Crosswalk for Frais Hand Sanitizer?
- RxCUI: 1039811 - ethanol 66 % Topical Gel
- RxCUI: 1039811 - ethanol 0.66 ML/ML 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".