NDC 63505-157 Fraicheur Verveine Antiperspirant And Deodorant Roll-on
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What is NDC 63505-157?
What are the uses for Fraicheur Verveine Antiperspirant And Deodorant Roll-on?
Which are Fraicheur Verveine Antiperspirant And Deodorant Roll-on UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V)
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (Active Moiety)
Which are Fraicheur Verveine Antiperspirant And Deodorant Roll-on 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:
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ETHER (UNII: 0F5N573A2Y)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETEARETH-33 (UNII: R42C2O714B)
- CETYL ALCOHOL (UNII: 936JST6JCN)
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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".