NDC 51769-089 Dove Antiperspirant
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51769-089?
What are the uses for Dove Antiperspirant?
Which are Dove Antiperspirant 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 Dove Antiperspirant 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL BENZOATE (UNII: N863NB338G)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PPG-14 BUTYL ETHER (UNII: R199TJT95T)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ACONITIC ACID (UNII: 93371T1BXP)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- ISOEUGENOL (UNII: 5M0MWY797U)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- STEARETH-100 (UNII: 4OH5W9UM87)
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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".