NDC 51770-110 Perfect Truth Cc Eye Broad Spectrum Spf 15 Olehenriksen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51770 - Ole Henriksen
- 51770-110 - Perfect Truth Cc Eye Broad Spectrum Spf 15
Product Packages
NDC Code 51770-110-02
Package Description: 1 TUBE in 1 CARTON / 7 mL in 1 TUBE (51770-110-01)
Product Details
What is NDC 51770-110?
What are the uses for Perfect Truth Cc Eye Broad Spectrum Spf 15 Olehenriksen?
Which are Perfect Truth Cc Eye Broad Spectrum Spf 15 Olehenriksen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Perfect Truth Cc Eye Broad Spectrum Spf 15 Olehenriksen 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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PROPANEDIOL (UNII: 5965N8W85T)
- COCO-GLYCERIDES (UNII: ISE9I7DNUG)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q)
- MICA (UNII: V8A1AW0880)
- SHEA BUTTER (UNII: K49155WL9Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- ISOSTEARYL HYDROXYSTEARATE (UNII: F7540880P0)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
* 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".