NDC 11559-769 Re-nutriv Intensive Liftng Make Up Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11559 - Estee Lauder Inc
- 11559-769 - Re-nutriv
Product Packages
NDC Code 11559-769-01
Package Description: 1 CONTAINER in 1 CARTON / 30 mL in 1 CONTAINER
Product Details
What is NDC 11559-769?
Which are Re-nutriv Intensive Liftng Make Up Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Re-nutriv Intensive Liftng Make Up Spf15 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)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- MILK THISTLE (UNII: 822I9LEJ7S)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CAFFEINE (UNII: 3G6A5W338E)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SUCROSE (UNII: C151H8M554)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- LAURETH-7 (UNII: Z95S6G8201)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ZINC STEARATE (UNII: H92E6QA4FV)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- IMIDUREA (UNII: M629807ATL)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- MICA (UNII: V8A1AW0880)
* 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".