NDC 59915-1001 Conju Princess Bb
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 59915-1001?
What are the uses for Conju Princess Bb?
Which are Conju Princess Bb UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ARBUTIN (UNII: C5INA23HXF)
- ARBUTIN (UNII: C5INA23HXF) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Conju Princess Bb 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)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- TALC (UNII: 7SEV7J4R1U)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- HECTORITE (UNII: 08X4KI73EZ)
- BENTONITE (UNII: A3N5ZCN45C)
- CHAMOMILE (UNII: FGL3685T2X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- ALLANTOIN (UNII: 344S277G0Z)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- LICORICE (UNII: 61ZBX54883)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- OCTYLTRIETHOXYSILANE (UNII: LDC331P08E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
* 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".