NDC 64942-1292 Suave Powder Antiperspirant And Deodorant
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What is NDC 64942-1292?
What are the uses for Suave Powder Antiperspirant And Deodorant?
Which are Suave Powder Antiperspirant And Deodorant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)
Which are Suave Powder Antiperspirant And 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:
- BUTANE (UNII: 6LV4FOR43R)
- 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- TALC (UNII: 7SEV7J4R1U)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- ISOBUTANE (UNII: BXR49TP611)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PROPANE (UNII: T75W9911L6)
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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".