NDC 14783-955 Lbel Dry Effect 48 Antiperspirant Deodorant Roll-on
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What is NDC 14783-955?
What are the uses for Lbel Dry Effect 48 Antiperspirant Deodorant Roll-on?
Which are Lbel Dry Effect 48 Antiperspirant 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 Lbel Dry Effect 48 Antiperspirant 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)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- TRICLOSAN (UNII: 4NM5039Y5X)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- LEVOMENOL (UNII: 24WE03BX2T)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ALCOHOL (UNII: 3K9958V90M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- THYME (UNII: CW657OBU4N)
- EDETATE SODIUM (UNII: MP1J8420LU)
- OREGANO (UNII: 0E5AT8T16U)
- CORN OIL (UNII: 8470G57WFM)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- INOSITOL (UNII: 4L6452S749)
- RETINOL (UNII: G2SH0XKK91)
- ROSEMARY (UNII: IJ67X351P9)
- ROSA MOSCHATA SEED OIL (UNII: T031ZE559T)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- LEMON PEEL (UNII: 72O054U628)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- STARCH, CORN (UNII: O8232NY3SJ)
- BIOTIN (UNII: 6SO6U10H04)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- COUMARIN (UNII: A4VZ22K1WT)
* Please review the disclaimer below.
[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".