NDC 66184-425 Ck One 3-in-1 Face Makeup With Spf 8 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66184 - Coty Us Llc
- 66184-425 - Ck One 3-in-1 Face Makeup
Product Packages
NDC Code 66184-425-01
Package Description: 30 mL in 1 CONTAINER
NDC Code 66184-425-02
Package Description: 30 mL in 1 BOX
NDC Code 66184-425-03
Package Description: 10 mL in 1 BOTTLE
Product Details
What is NDC 66184-425?
What are the uses for Ck One 3-in-1 Face Makeup With Spf 8 Sunscreen?
Which are Ck One 3-in-1 Face Makeup With Spf 8 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Ck One 3-in-1 Face Makeup With Spf 8 Sunscreen 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)
- NEOPENTYL GLYCOL (UNII: QI80HXD6S5)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- TRICAPRIN (UNII: O1PB8EU98M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYL METHACRYLATE (UNII: 196OC77688)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALUMINUM DIMYRISTATE (UNII: J2KA067N9O)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
- SORBIC ACID (UNII: X045WJ989B)
- ALARIA ESCULENTA (UNII: EJ9JK8J58D)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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[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".