NDC 64942-1224 Dove Cleartone Pink Antiperspirant Deodorant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64942 - Conopco Inc. D/b/a Unilever
- 64942-1224 - Dove
Product Packages
NDC Code 64942-1224-1
Package Description: 74 g in 1 CONTAINER
NDC Code 64942-1224-2
Package Description: 45 g in 1 CONTAINER
NDC Code 64942-1224-3
Package Description: 14 g in 1 CONTAINER
Product Details
What is NDC 64942-1224?
What are the uses for Dove Cleartone Pink Antiperspirant Deodorant?
Which are Dove Cleartone Pink Antiperspirant Deodorant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
- ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)
Which are Dove Cleartone Pink Antiperspirant Deodorant 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)
- PPG-14 BUTYL ETHER (UNII: R199TJT95T)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- STEARETH-100 (UNII: 4OH5W9UM87)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SOYBEAN OIL (UNII: 241ATL177A)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
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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".