NDC 80261-101 Lauren Conrad - The Liquid Foundation Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 80261-101?
What are the uses for Lauren Conrad - The Liquid Foundation Spf 15?
Which are Lauren Conrad - The Liquid Foundation Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Lauren Conrad - The Liquid Foundation Spf 15 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)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- GLYCERIN (UNII: PDC6A3C0OX)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)
- SHEA BUTTER (UNII: K49155WL9Y)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- BETAINE (UNII: 3SCV180C9W)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PHYTANTRIOL (UNII: 8LVI07A72W)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- LYSINE (UNII: K3Z4F929H6)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".