NDC 65105-001 Donna Karan Cashmere Mist Deodorant Anti-perspirant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65105 - Donna Karan Cosmetics Co.
- 65105-001 - Donna Karan Cashmere Mist Deodorant Anti-perspirant
Product Packages
NDC Code 65105-001-01
Package Description: 1 CANISTER in 1 CARTON / 50 mL in 1 CANISTER
Product Details
What is NDC 65105-001?
What are the uses for Donna Karan Cashmere Mist Deodorant Anti-perspirant?
Which are Donna Karan Cashmere Mist Deodorant Anti-perspirant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)
Which are Donna Karan Cashmere Mist Deodorant Anti-perspirant 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- PPG-14 BUTYL ETHER (UNII: R199TJT95T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TALC (UNII: 7SEV7J4R1U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
- ALLANTOIN (UNII: 344S277G0Z)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- BENZYL BENZOATE (UNII: N863NB338G)
- COUMARIN (UNII: A4VZ22K1WT)
- GERANIOL (UNII: L837108USY)
- ISOEUGENOL (UNII: 5M0MWY797U)
- EUGENOL (UNII: 3T8H1794QW)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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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".